Estrogen Receptor-β Gene Cytosine-Adenine (ESR2-CA) Repeat Polymorphism in Postmenopausal Colon Cancer
by
, , and
Naoko Honma
1,2,*,
Tomio Arai
3,
Yoko Matsuda
3,4,
Yosuke Fukunaga
5,
Masaaki Muramatsu
6,
Shinobu Ikeda
7,
Yuri Akishima-Fukasawa
1,
Noriko Yamamoto
2,8,
Hiroshi Kawachi
2,8,
Yuichi Ishikawa
2,9,
Kengo Takeuchi
2,8,10 and
Tetuo Mikami
1 1
Department of Pathology, Faculty of Medicine, Toho University, Omori-Nishi, Ota-ku, Tokyo 143-8540, Japan
2
Division of Pathology, Cancer Institute, Japanese Foundation for Cancer Research, Ariake, Koto-ku, Tokyo 135-8550, Japan
3
Department of Pathology, Tokyo Metropolitan Geriatric Hospital, Sakaecho, Itabashi-ku, Tokyo 173-0015, Japan
4
Oncology Pathology, Department of Pathology and Host-Defense, Faculty of Medicine, Kagawa University, Ikenobe, Miki-cho, Kita-gun, Kagawa 761-0793, Japan
5
Gastroenterological Center, Department of Gastroenterological Surgery, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Ariake, Koto-ku, Tokyo 135-8550, Japan
6
Diagnostics and Therapeutics of Intractable Diseases, Intractable Disease Research Center, Graduate School of Medicine, Juntendo University, Hongo, Bunkyo-ku, Tokyo 113-8421, Japan
7
Japan Agency for Medical Research and Development, Otemachi, Chiyoda-ku, Tokyo 100-0004, Japan
8
Department of Pathology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Ariake, Koto-ku, Tokyo 135-8550, Japan
9
Department of Pathology, International University of Health and Welfare, Mita, Minato-ku, Tokyo 103-8329, Japan
10
Pathology Project for Molecular Targets, Cancer Institute, Japanese Foundation for Cancer Research, Ariake, Koto-ku, Tokyo 135-8550, Japan
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2023, 24(5), 4502; https://doi.org/10.3390/ijms24054502
Submission received: 18 January 2023
/
Revised: 19 February 2023
/
Accepted: 22 February 2023
/
Published: 24 February 2023
(This article belongs to the Special Issue Estrogen Receptors and Metabolism in Human Diseases)
Abstract
:The pathobiological role of estrogen is controversial in colorectal cancer. Cytosine-adenine (CA) repeat in the estrogen receptor (ER)-β gene (ESR2-CA) is a microsatellite, as well as representative of ESR2 polymorphism. Though its function is unknown, we previously showed that a shorter allele (germline) increased the risk of colon cancer in older women, whereas it decreased it in younger postmenopausal women. ESR2-CA and ER-β expressions were examined in cancerous (Ca) and non-cancerous (NonCa) tissue pairs from 114 postmenopausal women, and comparisons were made considering tissue types, age/locus, and the mismatch repair protein (MMR) status. ESR2-CA repeats <22/≥22 were designated as ‘S’/‘L’, respectively, resulting in genotypes SS/nSS (=SL&LL). In NonCa, the rate of the SS genotype and ER-β expression level were significantly higher in right-sided cases of women ≥70 (≥70Rt) than in those in the others. A decreased ER-β expression in Ca compared with NonCa was observed in proficient-MMR, but not in deficient-MMR. In NonCa, but not in Ca, ER-β expression was significantly higher in SS than in nSS. ≥70Rt cases were characterized by NonCa with a high rate of SS genotype or high ER-β expression. The germline ESR2-CA genotype and resulting ER-β expression were considered to affect the clinical characteristics (age/locus/MMR status) of colon cancer, supporting our previous findings.
1. Introduction
Estrogens have attracted attention as factors affecting the risk and outcome of colorectal cancer (CRC) [1,2,3,4,5,6]. A large number of in vitro and in vivo studies have suggested the inhibitory role of estrogens against CRC [1,2,4,7,8], whereas a fewer, but significant, number of studies have reported unfavorable effects on CRC [6]. CRC characteristics are affected by sex, age, and tumor locus. The proportion of right-sided colon cancer increases as age increases, and is consistently higher in women than men regardless of age [6]. Histologically, the proportion of medullary/mucinous carcinoma (Med/Muc), which frequently locate right-sided, increases with age. Microsatellite instability (MSI), a representative carcinogenic mechanism caused by deficiency of mismatch repair protein (dMMR), is associated with CRC of women, right-sidedness, or Med/Muc histology. Further, the concentration of estrogens drastically fluctuates throughout a woman’s lifetime: much higher in premenopausal women, but much lower in postmenopausal women than men. In such context, a systematic study considering sex, age, tumor locus, or MMR status is needed to appropriately understand the pathobiological role of estrogens in CRC.
In normal colorectal epithelium, estrogen receptor (ER)-β, the second ER, is the main ER, suggesting that estrogen exerts its function through ER-β. ER-β expression has been reported to decrease according to canceration or cancer progression, suggesting that the estrogen-ER-β signaling malfunction is related to the carcinogenesis/development of CRC [1]. Further, expression of ER-β1, a wild type ER-β, has been reportedly higher in MSI-positive than MSI-negative CRC [1,9]. In an epidemiological study, estrogen has been suggested to reduce MSI-negative or ER-β-positive CRC, but not MSI-positive or ER-β-negative CRC [10,11]. These findings suggest that estrogen affects the tumor types generated, as well as behaves differently according to the status of MSI or ER-β.
We recently examined the estrogen concentration and expression of the estrogen receptor (ER)-β (the main ER in colorectum) in pairs of colon cancerous/non-cancerous tissues (Ca/NonCa) from postmenopausal women. In such a study setting, we could avoid the effect of gender difference or menopausal status, and could focus on the effect of age, tumor locus, or tumor type. ER-β reduction in Ca compared with its NonCa counterpart, which has been repeatedly reported, was observed only in left-sided cases involving patients younger than 70 y/o, cases with a non-medullary/mucinous (Med/Muc) histology, or MMR-proficient (pMMR) cases, suggesting that the inhibitory role of estrogens is limited to these types of tumors. By contrast, ER-β-positivity, higher estradiol (E2) concentration, dMMR, and Med/Muc histology were closely related to right-sided tumors in women 70 y/o or older (≥70Rt), and those factors were also closely related to each other, suggesting a promotive role of estrogens in these tumors [12]. Groups including ours previously reported that ER-β gene (ESR2) cytosine-adenine (CA) repeat polymorphism (ESR2-CA) [13] in the germline affected the colon cancer risk in postmenopausal women, but not rectal cancer risk, or colon cancer risk in men and premenopausal women [14,15,16]. Further, the risk of this polymorphism in postmenopausal colon cancer has been shown to invert with age: a shorter allele (S) was associated with a higher risk in older women, but a lower risk in younger postmenopausal women [14,15,16], suggesting a divergent pathogenic role of this polymorphism in postmenopausal colon cancer according to age.
ESR2-CA is one of the microsatellites. Microsatellites instability (MSI), a change in the repetition number of microsatellites in tumors, is caused by a deficiency of MMR. Lynch syndrome, or hereditary non-polyposis colorectal cancer (HNPCC), is well-known for its germline mutation; however, MMR-deficiency is also frequently noted in non-hereditary colon cancer in older women, with a right-sided locus, or with Med/Muc histology. Although the germline ESR2-CA and risk of colon cancer have been associated, as described above, the instability of this microsatellite in colon cancerous tissue has never been reported. The purpose of this study was to elucidate whether and how ESR2-CA or its instability affects colon cancer pathogenesis, considering the background of patients and tumors. We also examined the association between ESR2-CA and ER-β expression, which has also never been reported.
2. Results
2.1. Patient/Tumor Background
The association between the MMR status and patient/tumor background considering age and tumor locus is summarized in Table 1. The rate of dMMR was significantly different among four groups (≥70Rt, <70/right (<70Rt), ≥70/left (≥70Lt), and <70/left (<70Lt). p = 0.0023), and higher in ≥70Rt than in the other three groups, suggesting the specificity of ≥70Rt. These groups other than ≥70Rt were combined as Non(≥70Rt). The rate of dMMR was again significantly higher in ≥70Rt than in Non(≥70Rt) (p = 0.0005). Additionally, taking tissue categories (Ca and NonCa) and the MMR status (dMMR and pMMR) into consideration, we further categorized samples into eight groups, and comparisons were made among these groups in the following analyses.
2.2. ESR2-CA
2.2.1. Distribution of ESR2-CA Allele Frequency
The distribution of the ESR2-CA allele frequency in NonCa and Ca is shown in Figure 1. In both tissue categories, the number of ESR2 CA repeats was distributed from 14 to 26 with two major peaks at 18 and 23, which is largely consistent with the results of other studies in the Japanese population (Figure 1) [14,15,17]. Using the same cutoff as in previous Japanese studies [14,15,17], we designated the allele with CA repeats <22 as the ‘S’ allele and ≥22 as the ‘L’ allele (Figure 1), resulting in three genotypes, SS, SL, and LL. To simplify this, SL and LL were combined as ‘nSS’, and the subjects were divided into two genotype categories, ‘SS’ and ‘nSS’.
2.2.2. Change of ESR2-CA Repeat Number in Ca Compared with NonCa
A change in the number of CA repeats between NonCa and Ca was significantly more frequent in dMMR cases (14/18, 78%) than in pMMR cases (16/96, 17%) (p < 0.0001). In more detail, 10 of 14 ≥70Rt/dMMR (71%), 2 of 31 ≥70Rt/pMMR (6.4%), four of four Non(≥70Rt)/dMMR (100%), and 14 of 65 Non(≥70Rt)/pMMR (22%) exhibited change in the number of CA repeats between NonCa and Ca, yielding a significant difference among the four categories (p < 0.0001). To examine more precisely, we added the number of two ESR2-CA repeats in each sample to yield ‘total ESR2-CA repeat number’, and compared it between the pairs (NonCa and Ca) of each patient. The distribution of the difference of ‘total ESR2-CA repeat number’ between pairs was compared among the four categories (Figure 2). In ≥70Rt/dMMR, 10 of 14 exhibited −9 to +3, whereas only one each of ≥70Rt/pMMR showed +1 and −1. All 4 Non(≥70Rt)/dMMR exhibited a decrease in CA repeat number in tumors (−9 to −3), whereas 14 of 65 Non(≥70Rt)/pMMR showed various differences between pairs.
2.2.3. Comparison of ESR2-CA Genotype among Categories
The ESR2-CA genotype was compared among four groups categorized by the age/locus and MMR status in NonCa and Ca (Table 2). In NonCa, the proportion of SS was larger in ≥70Rt than in Non(≥70Rt) (p = 0.0007) irrespective of the MMR status. In Ca, the proportion of SS was also higher in ≥70Rt than in Non(≥70Rt); however, the difference was much less in Ca than in NonCa (p = 0.0515) because of cases with changes of the ESR2-CA genotype in Non(≥70Rt) tumors (nSS in NonCa to SS in Ca). The ESR2-CA genotype was also compared between Ca and NonCa among the same group categorized by age/locus and the MMR status. The proportion of SS was same between NonCa and Ca in ≥70Rt (p = 1.0000), but was insignificantly higher in Ca than NonCa among Non(≥70Rt) (p = 0.1096) (Table 2, Figure 3, above).
2.3. Expression of ER-β
Immunohistochemical ER-β expression (total score) was compared among eight groups categorized by tissue type, age/locus, and the MMR status (Figure 4). Among NonCa, ≥70Rt/dMMR and ≥70Rt/pMMR exhibited significantly higher ER-β expression than Non(≥70Rt)/pMMR. Among Ca, ≥70Rt/dMMR and ≥70Rt/pMMR again exhibited significantly higher ER-β expression than Non(≥70Rt)/pMMR, and furthermore, ER-β expression in ≥70Rt/dMMR was significantly higher than in ≥70Rt/pMMR. As for the comparison between NonCa and Ca, a significant decrease in Ca was observed in ≥70Rt/pMMR and Non(≥70Rt)/pMMR, but not in ≥70R/dMMR or Non(≥70Rt)/dMMR (Figure 3 (below) and Figure 4).
2.4. The Relation between ESR2-CA Genotype and ER-β Expression
Immunohistochemical ER-β expression (total score, TS) was compared between SS and nSS in NonCa and Ca. ER-β expression was significantly higher in SS than in nSS among NonCa, which was not true among Ca (Figure 5).
3. Discussion
In the present study, we examined the ESR2-CA and ER-β expression in NonCa and Ca of surgical materials from postmenopausal colon cancer patients, taking the patients’ age, tumor locus, and MMR status into consideration. This is the first study to systematically compare ESR2-CA, one of the microsatellites, between NonCa and Ca, and to compare it with ER-β expression. We observed that: (1) in NonCa, the rate of the ESR2-CA SS genotype and ER-β expression level were significantly higher in ≥70Rt than in Non(≥70Rt) irrespective of the MMR status (Table 2, Figure 3 and Figure 4). (2) In NonCa, ER-β expression was significantly higher in SS than in nSS, which was not true in Ca (Figure 5). (3) The ESR2-CA repeat number frequently differed between NonCa and Ca in dMMR, but not in pMMR, although the ESR2-CA genotype did not significantly differ between them irrespective of MMR status (Table 2, Figure 2 and Figure 3).
We previously showed that germline SS increased the risk of colon cancer in older women as opposed to younger postmenopausal women, in whom SS decreased the risk [14,15]. We also showed that most colon cancers in older women with the germline SS genotype were right-sided, and exhibited higher ER-β expression in Ca, as well as in NonCa, although the sample size was small [14]. These previous findings are consistent with the present results, whereby the frequency of the SS genotype and ER-β expression levels were high in ≥70Rt than Non(≥70Rt) irrespective of the tissue category (Table 2, Figure 3 and Figure 4). In NonCa, ER-β expression was significantly higher in SS than in nonSS (Figure 5), suggesting that ESR2-CA determines ER-β expression, which leads to estrogen activity, at least partly, in normal colon epithelium. An association between shorter ESR2-CA alleles and higher estrogen activity has been suggested by studies on bone mineral density or systemic lupus erythematosus (SLE) [18,19]. The biological role of ESR2-CA, which exists in intron 5 of the ESR2 locus, is not known at present; however, intronic microsatellite repeats have been suggested to alter gene transcription, mRNA splicing or translation, gene silencing, or interaction with coregulators [20]. Several isotypes are known for ER-β. Ligand binding domain (LBD) is coded by alternatively spliced exon 8 of ESR2, resulting in five different forms of ER-β: ER-β1 to ER-β5 [21,22]. ER-β1, the wild-type, can bind to estrogens and transduces their signals; however, ERβ2-5 variants, with a truncated form of this domain, lack binding ability and dominant negatively regulate estrogen signaling [23]. One of the attractive hypotheses is that, in NonCa, ESR2-CA SS (but not nSS) facilitates the alternative splicing of exon 8, increasing the expression of wild-type ER-β (ER-β1), which is recognized by clone PPG5/10 used in this study as the primary antibody against ER-β [18,24].
By contrast, in Ca, ER-β expression was not related to ESR2-CA, suggesting a disordered relation between them (Figure 5). In Ca with pMMR, despite unchanged ESR2-CA, ER-β expression was significantly lower than in NonCa irrespective of patients’ age, which was not true in Ca with dMMR where ER-β expression was stable. The finding that the ESR2-CA repeat number frequently changed in Ca with dMMR but not in Ca with pMMR is reasonable because ESR2-CA is one of the microsatellites, which are used as indicators of the MMR status (MSI). The change in the ESR2-CA repeat number, however, did not affect the ESR2-CA genotype in ≥70Rt/dMMR. Although the mechanisms of how ER-β expression is regulated in Ca is unclear, a decrease in the estrogen action may be pathogenically important in pMMR tumors, but not in dMMR tumors. In pMMR, a carcinogenic mechanism other than MMR might cause an abnormality which disturbs the normal transcription of ESR2.
Why was the rate of the ESR2-CA SS genotype or ER-β expression high in NonCa in ≥70Rt? One hypothesis is that the germline SS genotype and resulting higher ER-β expression predisposes NonCa in ≥70Rt to cancerization, which means SS/ER-β promotes carcinogenesis in ≥70Rt. The right-sided colon is generally thought to be affected by the environment more than the left-sided colon or rectum. NonCa in ≥70Rt is likely to be most affected by the environment because of longtime exposure according to age. We previously showed that the estrogen concentration was high in Ca in ≥70Rt. Longtime exposure to a high estrogen concentration, which also contributes to increased nuclear ER-β expression, may be pathogenically important for cancer in ≥70Rt. In an experimental study using a colon cancer cell line with low ER-β expression, compulsory ER-β expression decreased MMR [25]. The dMMR tumor in ≥70Rt is an attractive candidate to explain this hypothesis because it has the background of NonCa with the ESR2-CA SS genotype, high ER-β expression, and a high estrogen concentration. Another hypothesis is that SS/ER-β lowers the risk of ‘usual’ cancer at a younger age by delaying the onset or suppressing proliferation until an advanced age when cancer is finally diagnosed. The pMMR tumor in ≥70Rt is a candidate to explain the second hypothesis. Alternatively, both of these hypotheses may work in coordination to develop Ca in ≥70Rt (Figure 6). By contrast, in women with the nSS genotype, low ER-β expression and menopausal estrogen decreases may increase the risk of ‘usual’ type colon cancer soon after menopause, suggesting the protective role of estrogen against colon cancer as generally believed (Figure 6) [1,2,4,7,8].
We speculate that the SS genotype is prone to develop dMMR tumors in ≥70Rt through active estrogen-ER-β signaling, as described above. Estrogen was suggested to promote dMMR through hMLH1 promoter methylation in prostatic/ovarian carcinogenesis [26,27]; however, the mechanism by which estrogen promotes hMLH1 promoter methylation is unclear. The relationship between ESR2-CA repeat and methylation status is also unknown. It deserves further study to clarify these associations because dMMR-related CRC in older patients is mostly caused by hMLH1 promoter methylation.
Is a change of the ESR2-CA repeat number, one of MSI, important in the pathogenesis of colon cancer? In the present study, this MSI seems to be the result of MMR, and not pathogenically important for the disease, because it neither significantly affected ESR2-CA genotype nor related with ER-β expression in tumors.
In the present study, the germline ESR2-CA genotype and resulting ER-β expression/estrogen activity was suggested to affect the type of colon cancer generated or patients’ age. Further studies to clarify the precise mechanism are needed to control colon cancer by manipulating estrogen.
4. Materials and Methods
4.1. Subjects
Pathological materials and frozen samples (pairs of Ca and NonCa) from 114 postmenopausal Japanese women (≥70 y/o, n = 72; <70 and ≥55 y/o, n = 42) who underwent curative surgery for colon cancer without preoperative therapy between 2006 and 2013 were available for this study at the Department of Pathology, Tokyo Metropolitan Geriatric Hospital and Cancer Institute Hospital, Japanese Foundation for Cancer Research (Tokyo, Japan). Histological classification was based on the Japanese Classification of Colorectal, Appendiceal, and Anal Carcinoma [28].
4.2. Immunohistochemical Examination of ER-β and MMR
Immunostaining was performed for representative sections of formalin-fixed and paraffin-embedded tissue using an autostainer, BOND III (Leica Microsystems Ltd., Shanghai, China), as described elsewhere [12]. Briefly, an anti-ER-β1 mouse monoclonal antibody was used to detect ER-β (mouse, clone PPG5/10; Bio-Rad Laboratories, Hercules, CA, USA. X20). MMR was detected by monoclonal antibody for MLH1 (rabbit, clone EPR3894; Abcam plc., Cambridge, UK. X1000), MSH2 (mouse, clone G129-1129; BD Pharmingen, San Jose, CA, USA. X500), MSH6 (rabbit, clone EPR3945; GeneTex, Los Angeles, CA, USA. X200), and PMS2 (mouse, clone A16-4; BD Pharmingen. X100). Antigen retrieval was conducted using citrate buffer pH 6.0 for MLH1 and EDTA pH 9.0 for the others (100 °C, 20 min).
Nuclear immunoreactivity for each antibody was evaluated by NH and TM, independently. As there is no standard method for assessing ER-β expression in CRC, the Allred score routinely used in clinical practice for breast cancer was adopted for evaluation. Briefly, nuclear immunoreactivity for ER-β is estimated independently by summing the percentage score, PS, and intensity score, IS, of positively-stained cells (PS: 0%, 0; <1%, 1; <10%, 2; <33%, 3; <67%, 4; ≥67%, 5. IS: weak, 1; medium, 2; strong, 3). For MMR, the loss of the nuclear staining for each antibody (anti-MLH1, anti-MSH2, anti-MSH6, and anti-PMS2) was evaluated. Deficient-MMR (dMMR) was defined as the loss of at least one MMR. Discrepancies were resolved by joint review of the slides.
4.3. Examination of ESR2-CA
Deoxyribonucleic acid (DNA) samples were extracted from the pairs of Ca and NonCa frozen tissues from each patient by the phenol/chloroform method. ESR2-CA was determined by polymerase chain reaction (PCR) using fluorescein-labeled oligonucleotide primers designed to amplify the polymorphic (CA)n repeat in intron 5 of ESR2, as described elsewhere [14]. Briefly, the forward primer was labeled with hexachloro-6-carboxy fluorescein and used together with the tailed reverse primer (5′-FAM-GGT AAA CCA TGG TCT GTA CC-3′, 5′-tail-AAC AAA ATG TTG AAT GAG TGG G-3′). An ABI PRISM 3130 Genetic Analyzer (Applied Biosystems, INC., Foster City, CA, USA) was used for the analyses. Alleles of ESR2-CA are presented with the number of CA repeats. Using the same cut-off used in the previous studies, alleles with CA repeats <22 and ≥22 were designated as ‘S’ and ‘L’, respectively, resulting in genotypes SS, LS, and LL [14,15]. To simplify, genotypes ‘SL’ and ‘LL’ were combined as ‘nSS’, and the subjects were finally divided into two genotype categories, ‘SS’ and ‘nSS’. ESR2-CA (repeat number or genotype) was compared among each tissue pair (Ca vs. NonCa) or with ER-β expression, considering the background of patients/tumors.
4.4. Statistical Methods
The Tukey–Kramer method was used to compare the Allred score (total score, TS) for ER-β between tissue categories classified by tissue type (Ca or NonCa), age/locus category (≥70/right, ≥70Rt; or Non(≥70Rt)), or the MMR status (dMMR or pMMR). Fisher’s exact test using a contingency table was used to compare various nominal variables (ESR2-CA genotype or tissue/patient background). In all instances, the statistical software JMP version 12 (SAS Institute, Cary, NC, USA) was used. p < 0.05 was considered significant.
5. Conclusions
The ≥70Rt cases were characterized by NonCa with a higher rate of the ESR2-CA SS genotype or higher ER-β expression compared with Non(≥70Rt) cases. The germline ESR2-CA genotype and resulting ER-β expression/estrogen activity seem to affect the type of colon cancer generated or the age of onset/diagnosis of the disease. These may be a clue to resolving the controversy regarding the pathobiological role of estrogen in colorectal cancer.
Author Contributions
Conceptualization, N.H.; methodology, N.H., M.M. and S.I.; validation, Y.A.-F. and T.M.; formal analysis, N.H.; investigation, N.H.; resources, T.A., Y.F., N.Y., H.K., Y.I. and K.T.; data curation, N.H.; writing—original draft preparation, N.H.; writing—review and editing, T.A., Y.M., Y.F., M.M., S.I., Y.A.-F., N.Y., H.K., Y.I., K.T. and T.M.; visualization, N.H.; supervision, M.M., Y.I., K.T. and T.M.; project administration, N.H.; funding acquisition, N.H. All authors have read and agreed to the published version of the manuscript.
Funding
This study was supported by JSPS/MEXT KAKENHI (25460429, 21K06932).
Institutional Review Board Statement
This study was conducted in accordance with the Declaration of Helsinki, and approved by the ethics committee of Tokyo Metropolitan Geriatric Hospital (No. 260303) and Cancer Institute Hospital (No. 2012-1068&1069).
Informed Consent Statement
Informed opt-out consent was obtained from all subjects involved in the study.
Data Availability Statement
The data presented in this study are available on request from the corresponding author. The data are not publicly available due to ethical restrictions.
Acknowledgments
We thank all collaborative researchers involved in this study. We also thank Motoyoshi Iwakoshi, Tomoyo Kakita, Maho Yokoyama, and the technical staff of the Department of Pathology, Tokyo Metropolitan Geriatric Hospital and Cancer Institute, for their excellent technical support.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Kennelly, R.; Kavanagh, D.O.; Hogan, A.M.; Winter, D.C. Oestrogen and the Colon: Potential Mechanisms for Cancer Prevention. Lancet Oncol. 2008, 9, 385–391. [Google Scholar] [CrossRef] [PubMed]
- Barone, M.; Tanzi, S.; Lofano, K.; Scavo, M.P.; Guido, R.; Demarinis, L.; Principi, M.B.; Bucci, A.; Di Leo, A. Estrogens, Phytoestrogens and Colorectal Neoproliferative Lesions. Genes Nutr. 2008, 3, 7–13. [Google Scholar] [CrossRef] [PubMed]
- Barzi, A.; Lenz, A.M.; Labonte, M.J.; Lenz, H. Molecular Pathways: Estrogen Pathway in Colorectal Cancer. Clin. Cancer Res. 2013, 19, 5842–5848. [Google Scholar] [CrossRef] [PubMed]
- Maingi, J.W.; Tang, S.; Liu, S.; Ngenya, W.; Bao, E. Targeting Estrogen Receptors in Colorectal Cancer. Mol. Biol. Rep. 2020, 47, 4087–4091. [Google Scholar] [CrossRef]
- Abancens, M.; Bustos, V.; Harvey, H.; McBryan, J.; Harvey, B.J. Sexual Dimorphism in Colon Cancer. Front. Oncol. 2020, 10, 607909. [Google Scholar] [CrossRef]
- Honma, N.; Hosoi, T.; Arai, T.; Takubo, K. Estrogen and Cancers of the Colorectum, Breast, and Lung in Postmenopausal Women. Pathol. Int. 2015, 65, 451–459. [Google Scholar] [CrossRef]
- Cho, N.L.; Javid, S.H.; Carothers, A.M.; Redston, M.; Bertagnolli, M.M. Estrogen Receptors Alpha and Beta are Inhibitory Modifiers of Apc-Dependent Tumorigenesis in the Proximal Colon of Min/+ Mice. Cancer Res. 2007, 67, 2366–2372. [Google Scholar] [CrossRef]
- Saleiro, D.; Murillo, G.; Lubahn, D.B.; Kopelovich, L.; Korach, K.S.; Mehta, R.G. Enhanced Induction of Mucin-Depleted Foci in Estrogen Receptor {Beta} Knockout Mice. Cancer Prev. Res. 2010, 3, 1198–1204. [Google Scholar] [CrossRef]
- Wong, N.A.; Malcomson, R.D.; Jodrell, D.I.; Groome, N.P.; Harrison, D.J.; Saunders, P.T. ERbeta Isoform Expression in Colorectal Carcinoma: An in Vivo and in Vitro Study of Clinicopathological and Molecular Correlates. J. Pathol. 2005, 207, 53–60. [Google Scholar] [CrossRef]
- Limsui, D.; Vierkant, R.; Tillmans, L.S.; Wang, A.H.; Weisenberger, D.J.; Laird, P.W.; Lynch, C.F.; Anderson, K.E.; French, A.J.; Haile, R.W.; et al. Postmenopausal Hormone Therapy and Colorectal Cancer Risk by Molecularly Defined Subtypes among Older Women. Gut 2011, 61, 1299–1305. [Google Scholar] [CrossRef]
- Rudolph, A.; Toth, C.; Hoffmeister, M.; Roth, W.; Herpel, E.; Schirmacher, P.; Brenner, H.; Chang-Claude, J. Colorectal Cancer Risk Associated with Hormone use Varies by Expression of Estrogen Receptor-Β. Cancer Res. 2013, 73, 3306–3315. [Google Scholar] [CrossRef] [PubMed]
- Honma, N.; Arai, T.; Matsuda, Y.; Fukunaga, Y.; Akishima-Fukasawa, Y.; Yamamoto, N.; Kawachi, H.; Ishikawa, Y.; Takeuchi, K.; Mikami, T. Estrogen Concentration and Estrogen Receptor-Β Expression in Postmenopausal Colon Cancer Considering Patient/Tumor Background. J. Cancer Res. Clin. Oncol. 2022, 148, 1063–1071. [Google Scholar] [CrossRef]
- Ogawa, S.; Emi, M.; Shiraki, M.; Hosoi, T.; Ouchi, Y.; Inoue, S. Association of Estrogen Receptor Beta (ESR2) Gene Polymorphism with Blood Pressure. J. Hum. Genet. 2000, 45, 327–330. [Google Scholar] [CrossRef] [PubMed]
- Honma, N.; Arai, T.; Takubo, K.; Younes, M.; Tanaka, N.; Mieno, M.N.; Tamura, K.; Ikeda, S.; Sawabe, M.; Muramatsu, M. Oestrogen Receptor-Β CA Repeat Polymorphism is Associated with Incidence of Colorectal Cancer among Females. Histopathology 2011, 59, 216–224. [Google Scholar] [CrossRef] [PubMed]
- Honma, N.; Yamamoto, K.; Ohnaka, K.; Morita, M.; Toyomura, K.; Kono, S.; Muramatsu, M.; Arai, T.; Ueki, T.; Tanaka, M.; et al. Estrogen Receptor-Β Gene Polymorphism and Colorectal Cancer Risk: Effect Modified by Body Mass Index and Isoflavone Intake. Int. J. Cancer 2013, 132, 951–958. [Google Scholar] [CrossRef] [PubMed]
- Slattery, M.L.; Sweeney, C.; Murtaugh, M.; Ma, K.N.; Wolff, R.K.; Potter, J.D.; Caan, B.J.; Samowitz, W. Associations between ERalpha, ERbeta, and AR Genotypes and Colon and Rectal Cancer. Cancer Epidemiol. Biomark. Prev. 2005, 14, 2936–2942. [Google Scholar] [CrossRef] [PubMed]
- Takeo, C.; Negishi, E.; Nakajima, A.; Ueno, K.; Tatsuno, I.; Saito, Y.; Amano, K.; Hirai, A. Association of Cytosine-Adenine Repeat Polymorphism of the Estrogen Receptor-Beta Gene with Menopausal Symptoms. Gend. Med. 2005, 2, 96–105. [Google Scholar] [CrossRef]
- Scariano, J.K.; Simplicio, S.G.; Montoya, G.D.; Garry, P.J.; Baumgartner, R.N. Estrogen Receptor Beta Dinucleotide (CA) Repeat Polymorphism is significantly Associated with Bone Mineral Density in Postmenopausal Women. Calcif. Tissue Int. 2004, 74, 501–508. [Google Scholar] [CrossRef]
- Wang, J.; Nuite, M.; McAlindon, T.E. Association of Estrogen and Aromatase Gene Polymorphisms with Systemic Lupus Erythematosus. Lupus 2010, 19, 734–740. [Google Scholar] [CrossRef]
- Beleza-Meireles, A.; Kockum, I.; Lundberg, F.; Söderhäll, C.; Nordenskjöld, A. Risk Factors for Hypospadias in the Estrogen Receptor 2 Gene. J. Clin. Endocrinol. Metab. 2007, 92, 3712–3718. [Google Scholar] [CrossRef]
- Moore, J.T.; McKee, D.D.; Slentz-Kesler, K.; Moore, L.B.; Jones, S.A.; Horne, E.L.; Su, J.L.; Kliewer, S.A.; Lehmann, J.M.; Willson, T.M. Cloning and Characterization of Human Estrogen Receptor Beta Isoforms. Biochem. Biophys. Res. Commun. 1998, 247, 75–78. [Google Scholar] [CrossRef] [PubMed]
- Honma, N.; Matsuda, Y.; Mikami, T. Carcinogenesis of Triple-Negative Breast Cancer and Sex Steroid Hormones. Cancers 2021, 13, 2588. [Google Scholar] [CrossRef] [PubMed]
- Hamilton, N.; Marquez-Garban, D.; Mah, V.H.; Elshimali, Y.; Elashoff, D.; Garon, E.B.; Vadgama, J.; Pietras, R. Estrogen Receptor-Beta and the Insulin-Like Growth Factor Axis as Potential Therapeutic Targets for Triple-Negative Breast Cancer. Crit. Rev. Oncog. 2015, 20, 373–390. [Google Scholar] [CrossRef] [PubMed]
- Rudolph, A.; Shi, H.; Försti, A.; Hoffmeister, M.; Sainz, J.; Jansen, L.; Hemminki, K.; Brenner, H.; Chang-Claude, J. Repeat Polymorphisms in ESR2 and AR and Colorectal Cancer Risk and Prognosis: Results from a German Population-Based Case-Control Study. BMC Cancer 2014, 14, 817. [Google Scholar] [CrossRef] [PubMed]
- Zhai, R.; Wang, G.; Cai, K.; Tao, K.; Xu, F.; Zhang, W.; Wang, Z. Epigenetic Regulation of the ERbeta Gene on the Estrogen Signal Transfection Pathway in Colon Cancer Cells. J. Huazhong Univ. Sci. Technolog. Med. Sci. 2010, 30, 69–74. [Google Scholar] [CrossRef] [PubMed]
- Nishijima, Y.; Yoshida, T.; Nakamura, K.; Fukuda, T. hMLH1 Promoter Methylation Status Causes Different Expression Patterns of Estrogen Receptor Protein with Endometrial Lesion Progression. Rinsho Byori 2013, 61, 97–103. [Google Scholar]
- Treas, J.; Tyagi, T.; Singh, K.P. Chronic Exposure to Arsenic, Estrogen, and their Combination Causes Increased Growth and Transformation in Human Prostate Epithelial Cells Potentially by Hypermethylation-Mediated Silencing of MLH1. Prostate 2013, 73, 1660–1672. [Google Scholar] [CrossRef]
- Japanese Society for Cancer of the Colon and Rectum. Japanese Classification of Colorectal, Appendiceal, and Anal Carcinoma, 3rd ed.; Kanehara: Tokyo, Japan, 2019. [Google Scholar]
Figure 1.
The distribution of ESR2 cytosine-adenine (ESR2-CA) allele frequency in non-cancerous (NonCa) and cancerous (Ca) tissue, with boxplots. Two major peaks were observed at 18 and 23 in both tissue categories, which is largely consistent with the results of other studies in the Japanese population. Alleles with CA repeats <22 and ≥22 were designated as ‘S’ and ‘L’, respectively, resulting in genotypes SS, LS, and LL. Genotypes ‘SL’ and ‘LL’ were combined as ‘nSS’.
Figure 1.
The distribution of ESR2 cytosine-adenine (ESR2-CA) allele frequency in non-cancerous (NonCa) and cancerous (Ca) tissue, with boxplots. Two major peaks were observed at 18 and 23 in both tissue categories, which is largely consistent with the results of other studies in the Japanese population. Alleles with CA repeats <22 and ≥22 were designated as ‘S’ and ‘L’, respectively, resulting in genotypes SS, LS, and LL. Genotypes ‘SL’ and ‘LL’ were combined as ‘nSS’.
Figure 2.
The ‘total ESR2-CA repeat number’ in cancerous tissue (Ca) was compared with that in non-cancerous tissue (NonCa) in each patient. The distribution of the difference of ‘total ESR2-CA repeat number’ between Ca and NonCa was compared among four groups categorized by the age/locus and mismatch repair protein (MMR) status. dMMR, deficient-MMR; pMMR, proficient-MMR; ≥70Rt, right-sided case ≥ 70 y/o; Non(≥70Rt), other than ≥70Rt.
Figure 2.
The ‘total ESR2-CA repeat number’ in cancerous tissue (Ca) was compared with that in non-cancerous tissue (NonCa) in each patient. The distribution of the difference of ‘total ESR2-CA repeat number’ between Ca and NonCa was compared among four groups categorized by the age/locus and mismatch repair protein (MMR) status. dMMR, deficient-MMR; pMMR, proficient-MMR; ≥70Rt, right-sided case ≥ 70 y/o; Non(≥70Rt), other than ≥70Rt.
Figure 3.
Typical feature of ESR2 cytosine-adenine (ESR2-CA) genotype (above) and ER-β expression (below) according to the categories determined by patients’ age/tumor locus (right-sided case ≥70 y/o, ≥70Rt vs. the others, Non(≥70Rt)) and mismatch repair protein status (MMR-deficient, dMMR vs. MMR-proficient, pMMR). The number of ESR2-CA repeats frequently varied in dMMR tumors; however, no change was produced in the genotype in ≥70Rt/dMMR (*). A decrease of ER-β expression in Ca compared with NonCa was observed only in pMMR tumors. Ca, cancerous tissue; NonCa, non-cancerous tissue.
Figure 3.
Typical feature of ESR2 cytosine-adenine (ESR2-CA) genotype (above) and ER-β expression (below) according to the categories determined by patients’ age/tumor locus (right-sided case ≥70 y/o, ≥70Rt vs. the others, Non(≥70Rt)) and mismatch repair protein status (MMR-deficient, dMMR vs. MMR-proficient, pMMR). The number of ESR2-CA repeats frequently varied in dMMR tumors; however, no change was produced in the genotype in ≥70Rt/dMMR (*). A decrease of ER-β expression in Ca compared with NonCa was observed only in pMMR tumors. Ca, cancerous tissue; NonCa, non-cancerous tissue.
Figure 4.
Comparison of immunohistochemical ER-β expression (total score, TS) by boxplot among eight groups categorized by tissue type (Ca vs. NonCa), age/locus (≥70Rt vs. Non(≥70Rt)), and MMR status (dMMR vs. pMMR). White horizontal bar, median; black horizontal bar, medium. Ca, cancerous tissue; NonCa, non-cancerous tissue; ≥70Rt, right-sided case ≥ 70 y/o; Non(≥70Rt), other than ≥70Rt; dMMR, mismatch repair protein (MMR)-deficient; pMMR, MMR-proficient.
Figure 4.
Comparison of immunohistochemical ER-β expression (total score, TS) by boxplot among eight groups categorized by tissue type (Ca vs. NonCa), age/locus (≥70Rt vs. Non(≥70Rt)), and MMR status (dMMR vs. pMMR). White horizontal bar, median; black horizontal bar, medium. Ca, cancerous tissue; NonCa, non-cancerous tissue; ≥70Rt, right-sided case ≥ 70 y/o; Non(≥70Rt), other than ≥70Rt; dMMR, mismatch repair protein (MMR)-deficient; pMMR, MMR-proficient.
Figure 5.
The relation between ESR2 cytosine-adenine (ESR2-CA) genotype and ER-β expression (total score, TS) in non-cancerous (NonCa) and cancerous (Ca) tissues by boxplots. White horizontal bar, median; black horizontal bar, medium. In NonCa, but not in Ca, ER-β expression was significantly higher in SS than in nSS. Ca, cancerous tissue; NonCa, non-cancerous tissue.
Figure 5.
The relation between ESR2 cytosine-adenine (ESR2-CA) genotype and ER-β expression (total score, TS) in non-cancerous (NonCa) and cancerous (Ca) tissues by boxplots. White horizontal bar, median; black horizontal bar, medium. In NonCa, but not in Ca, ER-β expression was significantly higher in SS than in nSS. Ca, cancerous tissue; NonCa, non-cancerous tissue.
Figure 6.
General image of the relation between ESR2-CA genotype (SS or nSS) in NonCa, age at cancer diagnosis, and cancer type. ‘Usual Ca’, having characteristics such as left-sided or pMMR, is suppressed by estrogen, whereas ‘unusual Ca’, having characteristics such as right-sided or dMMR, is promoted by estrogen. Postmenopausal women with nSS genotype and lower ER-β expression in NonCa have a higher risk of usual Ca at a younger age, contrasting with those with the SS genotype, where more Ca are diagnosed at an older age due to slow onset/development of the disease. Ca, cancerous tissue; NonCa, non-cancerous tissue; dMMR, mismatch repair protein (MMR)-deficient; pMMR, MMR-proficient.
Figure 6.
General image of the relation between ESR2-CA genotype (SS or nSS) in NonCa, age at cancer diagnosis, and cancer type. ‘Usual Ca’, having characteristics such as left-sided or pMMR, is suppressed by estrogen, whereas ‘unusual Ca’, having characteristics such as right-sided or dMMR, is promoted by estrogen. Postmenopausal women with nSS genotype and lower ER-β expression in NonCa have a higher risk of usual Ca at a younger age, contrasting with those with the SS genotype, where more Ca are diagnosed at an older age due to slow onset/development of the disease. Ca, cancerous tissue; NonCa, non-cancerous tissue; dMMR, mismatch repair protein (MMR)-deficient; pMMR, MMR-proficient.
Table 1.
Status of mismatch repair protein (MMR) of postmenopausal colon cancer according to patients’ age and tumor locus.
Table 1.
Status of mismatch repair protein (MMR) of postmenopausal colon cancer according to patients’ age and tumor locus.
| dMMR n (%) | pMMR n (%) | p-Value | |
|---|---|---|---|
| ≥70Rt | 14 (31%) | 31 (69%) | 0.0005 S * |
| Non(≥70Rt) | 4 (6%) | 65 (94%) | |
| <70Rt | 2 (11%) | 17 (89%) | |
| ≥70Lt | 2 (7%) | 25 (93%) | 0.0023 S *† |
| <70Lt | 0 (0%) | 23 (100%) |
* Fisher’s exact test. † Comparison between four groups (≥70Rt, <70Rt, ≥70Lt, <70Lt). dMMR, deficient-MMR; pMMR, proficient-MMR; ≥70Rt, right-sided case ≥ 70 y/o; <70Rt, right-sided case < 70 y/o; ≥70Lt, left-sided case ≥ 70 y/o; <70Lt, left-sided case < 70 y/o; S, significant (p < 0.05). Non(≥70Rt) means <70Rt and ≥70Lt and <70Lt.
Table 2.
ESR2-CA repeat genotype category in non-cancerous (NonCa) or cancerous (Ca) tissue according to the patients’ age/locus and mismatch repair protein (MMR) status of tumors.
Table 2.
ESR2-CA repeat genotype category in non-cancerous (NonCa) or cancerous (Ca) tissue according to the patients’ age/locus and mismatch repair protein (MMR) status of tumors.
| ESR2-CA Repeat Genotype Category | |||||
|---|---|---|---|---|---|
| NonCa | Ca | ||||
| SS n (%) | nSS n (%) | SS n (%) | nSS n (%) | p-Value | |
| ≥70Rt ≥70Rt/dMMR ≥70Rt/pMMR | 22 (49%) 7 (50%) 15 (48%) | 23 (51%) 7 (50%) 16 (52%) | 22 (49%) 7 (50%) 15 (48%) | 23 (51%) 7 (50%) 16 (52%) | 1.0000 * 1.0000 * 1.0000 * |
| Non(≥70Rt) Non(≥70Rt)/dMMR Non(≥70Rt)/pMMR | 12 (17%) 1 (25%) 11 (17%) | 57 (83%) 3 (75%) 54 (83%) | 21 (30%) 3 (75%) 18 (28%) | 48 (70%) 1 (25%) 47 (72%) | 0.1096 * 0.4857 * 0.2058 * |
| p-value § p-value §§ | 0.0007 S* 0.0026 S* | 0.0515 * 0.0484 S* | |||
* Fisher’s exact test. dMMR, deficient-MMR; pMMR, proficient-MMR; ≥70Rt, right-sided case ≥70 y/o; Non(≥70Rt), other than ≥70Rt; S, significant (p < 0.05). § ≥70Rt vs. Non(≥70Rt), §§ Among ≥ 70Rt/dMMR, ≥70Rt/pMMR, Non(≥70Rt)/dMMR and Non(≥70Rt)/pMMR.
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Honma, N.; Arai, T.; Matsuda, Y.; Fukunaga, Y.; Muramatsu, M.; Ikeda, S.; Akishima-Fukasawa, Y.; Yamamoto, N.; Kawachi, H.; Ishikawa, Y.; et al. Estrogen Receptor-β Gene Cytosine-Adenine (ESR2-CA) Repeat Polymorphism in Postmenopausal Colon Cancer. Int. J. Mol. Sci. 2023, 24, 4502. https://doi.org/10.3390/ijms24054502
AMA Style
Honma N, Arai T, Matsuda Y, Fukunaga Y, Muramatsu M, Ikeda S, Akishima-Fukasawa Y, Yamamoto N, Kawachi H, Ishikawa Y, et al. Estrogen Receptor-β Gene Cytosine-Adenine (ESR2-CA) Repeat Polymorphism in Postmenopausal Colon Cancer. International Journal of Molecular Sciences. 2023; 24(5):4502. https://doi.org/10.3390/ijms24054502
Chicago/Turabian StyleHonma, Naoko, Tomio Arai, Yoko Matsuda, Yosuke Fukunaga, Masaaki Muramatsu, Shinobu Ikeda, Yuri Akishima-Fukasawa, Noriko Yamamoto, Hiroshi Kawachi, Yuichi Ishikawa, and et al. 2023. "Estrogen Receptor-β Gene Cytosine-Adenine (ESR2-CA) Repeat Polymorphism in Postmenopausal Colon Cancer" International Journal of Molecular Sciences 24, no. 5: 4502. https://doi.org/10.3390/ijms24054502
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