Next Article in Journal
Cardiac Computed Tomography Identification of the Septal Vein—A Small Retrospective Study
Previous Article in Journal
Malnutrition and the Post-Acute Sequelae of Severe Acute Respiratory Syndrome Coronavirus 2 Infection: A Multi-Institutional Population-Based Propensity Score-Matched Analysis
Previous Article in Special Issue
Eosinophilic Dermatoses: Cause of Non-Infectious Erythema after Volume Replacement with Diced Acellular Dermal Matrix in Breast Cancer?
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Editorial

Bridging Discoveries and Treatments: The New Landscape of Breast Cancer Research

by
Taobo Hu
1,*,
Lei Wang
2,*,
Riccardo Autelli
3,* and
Mengping Long
4,*
1
Department of Breast Surgery, Peking University People’s Hospital, Beijing 100033, China
2
International Cancer Center, Shenzhen University, Shenzhen 518060, China
3
Department of Clinical and Biological Sciences, University of Turin, 10125 Turin, Italy
4
Department of Pathology, Peking University Cancer Hospital, Beijing 100191, China
*
Authors to whom correspondence should be addressed.
Life 2024, 14(6), 747; https://doi.org/10.3390/life14060747
Submission received: 28 May 2024 / Accepted: 3 June 2024 / Published: 12 June 2024
(This article belongs to the Special Issue Advances in Breast Cancer Research and Treatment)
Welcome to our Special Issue, “Advances in Breast Cancer Research and Treatment” of Life, where we have embarked on a comprehensive exploration of groundbreaking studies that advance our understanding and management of breast cancer. Each paper contributes uniquely to the evolving landscape of breast cancer research, ranging from the clinicopathological characteristics of breast carcinoma with neuroendocrine features [1], the identification of hub genes in the context of non-alcoholic fatty liver disease and triple-negative breast cancer [2], to advancements in diagnostic techniques [3], and the exploration of immunotherapy biomarkers [4]. Some of the topics covered include innovative methods for breast cancer classification combining transfer learning and attention mechanisms [5] and the role of diffusion-weighted imaging in breast cancer diagnosis among young patients [6]. The collective insights presented here not only underscore the complexity of this disease but also highlight the promising pathways toward more effective treatments and improved patient outcomes.

1. Highlights from This Special Issue

1.1. Application of Deep Learning in Breast Cancer Pathology Image Classification

The article “Improved Breast Cancer Classification through Combining Transfer Learning and Attention Mechanism” introduces a novel approach that enhances the accuracy and interpretability of breast cancer histopathological image classification [5]. This method utilizes modified pre-trained Convolutional Neural Network (CNN) models and attention mechanisms to emphasize localized features and enable accurate discrimination in complex cases.

1.2. The Use of Diffusion-Weighted Imaging (DWI) in Young Breast Cancer Patients

“The Role of Diffusion-Weighted Imaging Based on Maximum-Intensity Projection in Young Patients with Marked Background Parenchymal Enhancement on Contrast-Enhanced Breast MRI” explores the application of DWI, particularly in young patients with significant background parenchymal enhancement (BPE) on contrast-enhanced MRI (CE-MRI) [6]. This study found that DWI outperforms CE-MRI in terms of lesion detection.

1.3. Association between Non-Alcoholic Fatty Liver Disease (NAFLD) and Triple-Negative Breast Cancer (TNBC)

The article titled “Identification of Hub Genes and Biological Mechanisms Associated with Non-Alcoholic Fatty Liver Disease and Triple-Negative Breast Cancer” identified hub genes associated with NAFLD and TNBC by analyzing publicly available transcriptomic data [2]. This study also explored the potential co-pathogenesis and prognostic linkage between these two diseases.

1.4. Breast Cancer Exposomics

The review titled “Breast Cancer Exposomics” discusses the impact of environmental exposures on the development of breast cancer, including the roles of environmental toxins, dietary components, psychosocial stressors, and their associated biological processes and molecular pathways [7]. This review emphasized the role of food and nutrition, as well as endocrine-disrupting chemicals (EDCs), in breast cancer development.

1.5. The Foundational Role of Breast Cancer Cell Lines in Cancer Research

“Molecular, Cellular, and Technical Aspects of Breast Cancer Cell Lines as a Foundational Tool in Cancer Research” reviews the history and origins of breast cancer cell lines and analyzes the molecular pathways that pharmaceutical drugs apply to these cell lines in vitro and in vivo [8]. This review also discussed controversies regarding the use of patient-derived xenografts (PDXs) versus cell-derived xenograft (CDXs) and 2D versus 3D cell culturing techniques.

1.6. Progress and Challenges of Immunotherapy Predictive Biomarkers for Triple-Negative Breast Cancer

“Progress and Challenges of Immunotherapy Predictive Biomarkers for Triple Negative Breast Cancer in the Era of Single-Cell Multi-Omics” discusses the advancements in single-cell sequencing techniques that have allowed for a deeper exploration of the complex and heterogeneous TNBC tumor microenvironment [4]. This review highlighted the potential of single-cell multi-omics analysis for identifying more effective biomarkers and personalized treatment strategies for TNBC patients.

1.7. Adverse Events of PD-1 or PD-L1 Inhibitors in Triple-Negative Breast Cancer

“Adverse Events of PD-1 or PD-L1 Inhibitors in Triple-Negative Breast Cancer: A Systematic Review and Meta-Analysis” provides a comprehensive understanding of treatment-related adverse events when using PD-1 or PD-L1 inhibitors in TNBC [9]. This study included an analysis of the incidence of serious immune-related adverse events and suggested considerations for their management.

1.8. In Silico Analysis of Triple-Negative Breast Cancer-Specific Biomarkers

“In Silico Analysis of Publicly Available Transcriptomic Data for the Identification of Triple-Negative Breast Cancer-Specific Biomarkers” employed in silico analyses to identify biomarkers for triple-negative breast cancer (TNBC), a subtype with limited treatment options [10]. Using publicly available transcriptomic data, the researchers of this study identified 34 differentially expressed genes (DEGs) associated with TNBC. These findings could help in developing targeted therapies and improving diagnostic accuracy.

1.9. Neuroendocrine Breast Carcinoma: Characteristics and Prognosis

“Clinicopathological Characteristics and Prognostic Profiles of Breast Carcinoma with Neuroendocrine Features” examined the clinicopathological characteristics and prognostic outcomes of breast carcinoma with neuroendocrine features [1]. This study found that these tumors are generally hormone receptor-positive and have a higher prevalence among postmenopausal women. Factors such as diabetes and advanced disease stage were associated with poorer progression-free survival.

1.10. Advancements in Post-Mastectomy Breast Reconstruction

“Breast Reconstruction following Mastectomy for Breast Cancer or Prophylactic Mastectomy: Therapeutic Options and Results” discusses various reconstructive options following mastectomy for breast cancer or as a preventive measure [11]. It highlights the evolution of techniques and materials that offer women more choices for breast restoration, aiming to improve psychological outcomes and quality of life after surgery.

1.11. Artificial Intelligence in Breast Cancer Diagnosis: Patient Perspectives

“Patients’ Perceptions and Attitudes to the Use of Artificial Intelligence in Breast Cancer Diagnosis: A Narrative Review” synthesizes patient perspectives on the use of artificial intelligence (AI) in breast cancer diagnostics [3]. It reveals that while there is interest in AI’s potential to improve diagnostic accuracy, there is also significant concern regarding trust and the desire for human oversight in the diagnostic process.

1.12. Investigating the Role of Eosinophils in Reactive Breast Stroma

“Eosinophilic Dermatoses: Cause of Non-Infectious Erythema after Volume Replacement with Diced Acellular Dermal Matrix in Breast Cancer?” explores the role of eosinophils in reactive breast stroma, particularly in the context of inflammation and tumor microenvironment interactions [12]. The findings of this study suggested that eosinophils may play a part in the breast’s response to tumor presence, although their exact role remains to be fully understood.

2. Advancing Frontlines: New Perspectives in Breast Cancer Research

Currently, several critical areas in breast cancer research are drawing considerable attention. Among them, significant advancements in immunotherapy, particularly for TNBC, are at the forefront [13]. TNBC is known for its aggressive nature and lack of targeted therapies, which makes the development of effective immunotherapy treatments especially crucial [14]. These treatments aim to harness the body’s immune system to better recognize and combat cancer cells, offering new hope for improving survival rates in a subgroup of breast cancer that has traditionally been challenging to treat [15]. Recent studies have highlighted the effectiveness of treatments like pembrolizumab, which, when combined with chemotherapy, has shown to improve survival rates in patients with high-risk early-stage TNBC [16,17].
Another major area of focus is the management of HER2-positive breast cancer. This subtype, characterized by the overexpression of the HER2 protein, has seen transformative treatments in recent decades, such as targeted therapies that significantly improve patient outcomes [18]. Research is ongoing to enhance these therapies’ efficacy and reduce side effects, ensuring more patients can benefit from these advanced treatments [19,20].
Additionally, the role and optimization of radiotherapy in breast cancer treatment protocols remain critical [21]. Radiotherapy is a cornerstone of breast cancer management, used both in the early and more advanced stages of this disease [22]. Innovations in radiotherapy techniques aim to increase the precision and effectiveness of radiation delivery, minimize damage to surrounding healthy tissues, and enhance its cancer-killing capabilities [23,24].
These research topics reflect a concerted and multidisciplinary effort to improve patient survival rates, manage risk factors more effectively, and refine surgical and chemotherapy strategies to offer tailored and less invasive treatment options. By pushing the boundaries in these key areas, researchers hope to not only extend the lives of those diagnosed with breast cancer but also improve their quality of life during and after treatment [25].

3. Final Reflections

This Special Issue embodies our collective quest to understand the complexities of breast cancer through cutting-edge research and to translate these discoveries into actionable treatments that improve patient outcomes. Through a multidisciplinary lens, we explore innovative diagnostic tools [5,10], breakthrough therapies [4,9], and pioneering surgical techniques [11] that are reshaping the way we approach this disease. Our contributors, leading experts in their fields, offer insights into the evolving paradigms of breast cancer management, from molecular genetics to personalized medicine. Their work not only reflects the current state of knowledge but also charts a course for future research directions. We invite you to delve into these pages, where the synergy of scientific discovery and clinical excellence illuminates the path toward a world with more effective breast cancer treatments.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Qiu, Y.; Dai, Y.; Zhu, L.; Hao, X.; Zhang, L.; Bao, B.; Chen, Y.; Wang, J. Clinicopathological Characteristics and Prognostic Profiles of Breast Carcinoma with Neuroendocrine Features. Life 2023, 13, 532. [Google Scholar] [CrossRef]
  2. Zhu, J.; Min, N.; Gong, W.; Chen, Y.; Li, X. Identification of Hub Genes and Biological Mechanisms Associated with Non-Alcoholic Fatty Liver Disease and Triple-Negative Breast Cancer. Life 2023, 13, 998. [Google Scholar] [CrossRef] [PubMed]
  3. Pesapane, F.; Giambersio, E.; Capetti, B.; Monzani, D.; Grasso, R.; Nicosia, L.; Rotili, A.; Sorce, A.; Meneghetti, L.; Carriero, S.; et al. Patients’ Perceptions and Attitudes to the Use of Artificial Intelligence in Breast Cancer Diagnosis: A Narrative Review. Life 2024, 14, 454. [Google Scholar] [CrossRef] [PubMed]
  4. Yu, J.; Guo, Z.; Wang, L. Progress and Challenges of Immunotherapy Predictive Biomarkers for Triple Negative Breast Cancer in the Era of Single-Cell Multi-Omics. Life 2023, 13, 1189. [Google Scholar] [CrossRef] [PubMed]
  5. Ashurov, A.; Chelloug, S.A.; Tselykh, A.; Muthanna, M.S.A.; Muthanna, A.; Al-Gaashani, M. Improved Breast Cancer Classification through Combining Transfer Learning and Attention Mechanism. Life 2023, 13, 1945. [Google Scholar] [CrossRef] [PubMed]
  6. Park, G.E.; Kang, B.J.; Kim, S.H.; Jung, N.Y. The Role of Diffusion-Weighted Imaging Based on Maximum-Intensity Projection in Young Patients with Marked Background Parenchymal Enhancement on Contrast-Enhanced Breast MRI. Life 2023, 13, 1744. [Google Scholar] [CrossRef] [PubMed]
  7. Neagu, A.N.; Jayaweera, T.; Corrice, L.; Johnson, K.; Darie, C.C. Breast Cancer Exposomics. Life 2024, 14, 402. [Google Scholar] [CrossRef] [PubMed]
  8. Witt, B.L.; Tollefsbol, T.O. Molecular, Cellular, and Technical Aspects of Breast Cancer Cell Lines as a Foundational Tool in Cancer Research. Life 2023, 13, 2311. [Google Scholar] [CrossRef] [PubMed]
  9. Zhang, Y.; Wang, J.; Hu, T.; Wang, H.; Long, M.; Liang, B. Adverse Events of PD-1 or PD-L1 Inhibitors in Triple-Negative Breast Cancer: A Systematic Review and Meta-Analysis. Life 2022, 12, 1990. [Google Scholar] [CrossRef]
  10. Kaddoura, R.; Alqutami, F.; Asbaita, M.; Hachim, M. In Silico Analysis of Publicly Available Transcriptomic Data for the Identification of Triple-Negative Breast Cancer-Specific Biomarkers. Life 2023, 13, 422. [Google Scholar] [CrossRef]
  11. Simion, L.; Petrescu, I.; Chitoran, E.; Rotaru, V.; Cirimbei, C.; Ionescu, S.O.; Stefan, D.C.; Luca, D.; Stanculeanu, D.L.; Gheorghe, A.S.; et al. Breast Reconstruction following Mastectomy for Breast Cancer or Prophylactic Mastectomy: Therapeutic Options and Results. Life 2024, 14, 138. [Google Scholar] [CrossRef] [PubMed]
  12. Schneider, J.; Lim, S.T.; Yi An, Y.; Suh, Y.J. Eosinophilic Dermatoses: Cause of Non-Infectious Erythema after Volume Replacement with Diced Acellular Dermal Matrix in Breast Cancer? Life 2024, 14, 608. [Google Scholar] [CrossRef] [PubMed]
  13. Onkar, S.S.; Carleton, N.M.; Lucas, P.C.; Bruno, T.C.; Lee, A.V.; Vignali, D.A.A.; Oesterreich, S. The Great Immune Escape: Understanding the Divergent Immune Response in Breast Cancer Subtypes. Cancer Discov. 2023, 13, 23–40. [Google Scholar] [CrossRef] [PubMed]
  14. Liu, Y.; Hu, Y.; Xue, J.; Li, J.; Yi, J.; Bu, J.; Zhang, Z.; Qiu, P.; Gu, X. Advances in immunotherapy for triple-negative breast cancer. Mol. Cancer 2023, 22, 145. [Google Scholar] [CrossRef] [PubMed]
  15. Leon-Ferre, R.A.; Goetz, M.P. Advances in systemic therapies for triple negative breast cancer. BMJ 2023, 381, e071674. [Google Scholar] [CrossRef] [PubMed]
  16. Tarantino, P.; Corti, C.; Schmid, P.; Cortes, J.; Mittendorf, E.A.; Rugo, H.; Tolaney, S.M.; Bianchini, G.; Andre, F.; Curigliano, G. Immunotherapy for early triple negative breast cancer: Research agenda for the next decade. NPJ Breast Cancer 2022, 8, 23. [Google Scholar] [CrossRef] [PubMed]
  17. Schmid, P.; Cortes, J.; Dent, R.; Pusztai, L.; McArthur, H.; Kummel, S.; Bergh, J.; Denkert, C.; Park, Y.H.; Hui, R.; et al. Event-free Survival with Pembrolizumab in Early Triple-Negative Breast Cancer. N. Engl. J. Med. 2022, 386, 556–567. [Google Scholar] [CrossRef] [PubMed]
  18. Marra, A.; Chandarlapaty, S.; Modi, S. Management of patients with advanced-stage HER2-positive breast cancer: Current evidence and future perspectives. Nat. Rev. Clin. Oncol. 2024, 21, 185–202. [Google Scholar] [CrossRef]
  19. Hurvitz, S.A.; Hegg, R.; Chung, W.P.; Im, S.A.; Jacot, W.; Ganju, V.; Chiu, J.W.Y.; Xu, B.; Hamilton, E.; Madhusudan, S.; et al. Trastuzumab deruxtecan versus trastuzumab emtansine in patients with HER2-positive metastatic breast cancer: Updated results from DESTINY-Breast03, a randomised, open-label, phase 3 trial. Lancet 2023, 401, 105–117. [Google Scholar] [CrossRef]
  20. Squifflet, P.; Saad, E.D.; Loibl, S.; van Mackelenbergh, M.T.; Untch, M.; Rastogi, P.; Gianni, L.; Schneeweiss, A.; Conte, P.; Piccart, M.; et al. Re-Evaluation of Pathologic Complete Response as a Surrogate for Event-Free and Overall Survival in Human Epidermal Growth Factor Receptor 2-Positive, Early Breast Cancer Treated With Neoadjuvant Therapy Including Anti-Human Epidermal Growth Factor Receptor 2 Therapy. J. Clin. Oncol. 2023, 41, 2988–2997. [Google Scholar] [CrossRef]
  21. Coles, C.E.; Haviland, J.S.; Kirby, A.M.; Griffin, C.L.; Sydenham, M.A.; Titley, J.C.; Bhattacharya, I.; Brunt, A.M.; Chan, H.Y.C.; Donovan, E.M.; et al. Dose-escalated simultaneous integrated boost radiotherapy in early breast cancer (IMPORT HIGH): A multicentre, phase 3, non-inferiority, open-label, randomised controlled trial. Lancet 2023, 401, 2124–2137. [Google Scholar] [CrossRef] [PubMed]
  22. Meattini, I.; Becherini, C.; Caini, S.; Coles, C.E.; Cortes, J.; Curigliano, G.; de Azambuja, E.; Isacke, C.M.; Harbeck, N.; Kaidar-Person, O.; et al. International multidisciplinary consensus on the integration of radiotherapy with new systemic treatments for breast cancer: European Society for Radiotherapy and Oncology (ESTRO)-endorsed recommendations. Lancet Oncol. 2024, 25, e73–e83. [Google Scholar] [CrossRef] [PubMed]
  23. Demircan, N.V.; Bese, N. New Approaches in Breast Cancer Radiotherapy. Eur. J. Breast Health 2024, 20, 1–7. [Google Scholar] [CrossRef] [PubMed]
  24. Sigurdson, S.; Thibodeau, S.; Korzeniowski, M.; Moraes, F.Y. A Precise Approach for Radiotherapy of Breast Cancer. Cancer Treat. Res. 2023, 188, 175–198. [Google Scholar] [CrossRef]
  25. Coles, C.E.; Earl, H.; Anderson, B.O.; Barrios, C.H.; Bienz, M.; Bliss, J.M.; Cameron, D.A.; Cardoso, F.; Cui, W.; Francis, P.A.; et al. The Lancet Breast Cancer Commission. Lancet 2024, 403, 1895–1950. [Google Scholar] [CrossRef]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Hu, T.; Wang, L.; Autelli, R.; Long, M. Bridging Discoveries and Treatments: The New Landscape of Breast Cancer Research. Life 2024, 14, 747. https://doi.org/10.3390/life14060747

AMA Style

Hu T, Wang L, Autelli R, Long M. Bridging Discoveries and Treatments: The New Landscape of Breast Cancer Research. Life. 2024; 14(6):747. https://doi.org/10.3390/life14060747

Chicago/Turabian Style

Hu, Taobo, Lei Wang, Riccardo Autelli, and Mengping Long. 2024. "Bridging Discoveries and Treatments: The New Landscape of Breast Cancer Research" Life 14, no. 6: 747. https://doi.org/10.3390/life14060747

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop