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Correction

Correction: del Molino del Barrio et al. Breast Cancer: An Examination of the Potential of ACKR3 to Modify the Response of CXCR4 to CXCL12. Int. J. Mol. Sci. 2018, 19, 3592

1
Applied Immunobiology and Transplantation Group, Institute of Cellular Medicine, Medical School, University of Newcastle upon Tyne, Newcastle upon Tyne NE2 4HH, UK
2
Institute of Genetic Medicine, International Centre for Life, University of Newcastle upon Tyne, Newcastle upon Tyne NE1 3BZ, UK
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2023, 24(23), 17108; https://doi.org/10.3390/ijms242317108
Submission received: 3 November 2023 / Accepted: 15 November 2023 / Published: 4 December 2023
(This article belongs to the Section Biochemistry)
The authors and Editorial Office were made aware of an error in a figure within the original publication [1].
During the compilation of the images for this article, an error occurred whereby the incorrect images for Figure 1, “no primary” antibody control for Patient 1 and 2, were published. The authors provided the correct original image files to the Editorial Office, and Figure 1 has now been updated with the correct “no primary” Patient 1 and 2 images. The magnification is different for the Patient 1 and 2 no primary controls. The authors state that the scientific conclusions are unaffected. This correction process was supervised and approved by the Academic Editor.

Reference

  1. del Molino del Barrio, I.; Wilkins, G.C.; Meeson, A.; Ali, S.; Kirby, J.A. Breast Cancer: An Examination of the Potential of ACKR3 to Modify the Response of CXCR4 to CXCL12. Int. J. Mol. Sci. 2018, 19, 3592. [Google Scholar] [CrossRef] [PubMed]
Figure 1. CXCR4 and ACKR3 staining using IHC in breast cancer tissue. Sections 4 μm in size from human breast cancer were stained for CXCR4 (1:40) and ACKR3 (1:100) using immunohistochemistry following no pre-treatment or EDTA antigen retrieval pre-treatment, respectively. Briefly, the protocol from the VECTASTAIN ABC HRP kit was followed; the signal was developed using DAB and counterstained with haematoxylin. No primary antibody was used as a control. n = 2, patient 1 control, scale bar = 100 μm; patient 2 control, scale bar = 200 μm.
Figure 1. CXCR4 and ACKR3 staining using IHC in breast cancer tissue. Sections 4 μm in size from human breast cancer were stained for CXCR4 (1:40) and ACKR3 (1:100) using immunohistochemistry following no pre-treatment or EDTA antigen retrieval pre-treatment, respectively. Briefly, the protocol from the VECTASTAIN ABC HRP kit was followed; the signal was developed using DAB and counterstained with haematoxylin. No primary antibody was used as a control. n = 2, patient 1 control, scale bar = 100 μm; patient 2 control, scale bar = 200 μm.
Ijms 24 17108 g001
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MDPI and ACS Style

del Molino del Barrio, I.; Wilkins, G.C.; Meeson, A.; Ali, S.; Kirby, J.A. Correction: del Molino del Barrio et al. Breast Cancer: An Examination of the Potential of ACKR3 to Modify the Response of CXCR4 to CXCL12. Int. J. Mol. Sci. 2018, 19, 3592. Int. J. Mol. Sci. 2023, 24, 17108. https://doi.org/10.3390/ijms242317108

AMA Style

del Molino del Barrio I, Wilkins GC, Meeson A, Ali S, Kirby JA. Correction: del Molino del Barrio et al. Breast Cancer: An Examination of the Potential of ACKR3 to Modify the Response of CXCR4 to CXCL12. Int. J. Mol. Sci. 2018, 19, 3592. International Journal of Molecular Sciences. 2023; 24(23):17108. https://doi.org/10.3390/ijms242317108

Chicago/Turabian Style

del Molino del Barrio, Irene, Georgina C. Wilkins, Annette Meeson, Simi Ali, and John A. Kirby. 2023. "Correction: del Molino del Barrio et al. Breast Cancer: An Examination of the Potential of ACKR3 to Modify the Response of CXCR4 to CXCL12. Int. J. Mol. Sci. 2018, 19, 3592" International Journal of Molecular Sciences 24, no. 23: 17108. https://doi.org/10.3390/ijms242317108

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