Ret Receptor Has Distinct Alterations and Functions in Breast Cancer
- PMID: 32080788
- DOI: 10.1007/s10911-020-09445-4
Ret Receptor Has Distinct Alterations and Functions in Breast Cancer
Abstract
Ret receptor tyrosine kinase is a proto-oncogene that participates in development of various cancers. Several independent studies have recently identified Ret as a key player in breast cancer. Although Ret overexpression and function have been under investigation, mainly in estrogen receptor positive breast cancer, a more comprehensive analysis of the impact of recurring Ret alterations in breast cancer is needed. This review consolidates the current knowledge of Ret alterations and their potential effects in breast cancer. We discuss and integrate data on Ret changes in different breast cancer subtypes and potential function in progression, as well as the participation of distinct Ret network signaling partners in these processes. We propose that it will be essential to define a shared molecular feature of tumors with alteration in Ret receptor, be this at the genetic level or via overexpression in order to design effective therapies to target the Ret pathway. Here we review experimental evidence from basic research and pre-clinical studies concentrating on Ret alterations as potential biomarkers for recurrence, and we discuss the possibility that targeting the Ret pathway might in the future become a treatment for breast cancer.
Keywords: Breast tumors; ER +; Endocrine resistance; Rearrangements; Ret.
Similar articles
-
Expression of RET is associated with Oestrogen receptor expression but lacks prognostic significance in breast cancer.BMC Cancer. 2019 Jan 8;19(1):41. doi: 10.1186/s12885-018-5262-0. BMC Cancer. 2019. PMID: 30621641 Free PMC article.
-
ER-positive breast cancer cells are poised for RET-mediated endocrine resistance.PLoS One. 2018 Apr 2;13(4):e0194023. doi: 10.1371/journal.pone.0194023. eCollection 2018. PLoS One. 2018. PMID: 29608602 Free PMC article.
-
High expression of the RET receptor tyrosine kinase and its ligand GDNF identifies a high-risk subset of estrogen receptor positive breast cancer.Breast Cancer Res Treat. 2023 Jun;199(3):589-601. doi: 10.1007/s10549-023-06937-9. Epub 2023 Apr 15. Breast Cancer Res Treat. 2023. PMID: 37061618 Free PMC article.
-
RET in breast cancer: functional and therapeutic implications.Trends Mol Med. 2011 Mar;17(3):149-57. doi: 10.1016/j.molmed.2010.12.007. Epub 2011 Jan 19. Trends Mol Med. 2011. PMID: 21251878 Review.
-
RET signaling in breast cancer therapeutic resistance and metastasis.Breast Cancer Res. 2023 Mar 14;25(1):26. doi: 10.1186/s13058-023-01622-7. Breast Cancer Res. 2023. PMID: 36918928 Free PMC article. Review.
Cited by
-
REThinking the role of the RET oncogene in breast cancer.Front Oncol. 2024 Aug 1;14:1427228. doi: 10.3389/fonc.2024.1427228. eCollection 2024. Front Oncol. 2024. PMID: 39211557 Free PMC article. Review.
-
RET overexpression leads to increased brain metastatic competency in luminal breast cancer.J Natl Cancer Inst. 2024 Oct 1;116(10):1632-1644. doi: 10.1093/jnci/djae091. J Natl Cancer Inst. 2024. PMID: 38852945 Free PMC article.
-
Aberrant RET expression affects normal mammary gland post-lactation transition, enhancing cancer potential.Dis Model Mech. 2022 Mar 1;15(3):dmm049286. doi: 10.1242/dmm.049286. Epub 2022 Mar 29. Dis Model Mech. 2022. PMID: 35044452 Free PMC article.
-
RET Gene Fusions in Malignancies of the Thyroid and Other Tissues.Genes (Basel). 2020 Apr 15;11(4):424. doi: 10.3390/genes11040424. Genes (Basel). 2020. PMID: 32326537 Free PMC article. Review.
-
JMJD6 orchestrates a transcriptional program in favor of endocrine resistance in ER+ breast cancer cells.Front Endocrinol (Lausanne). 2022 Nov 7;13:1028616. doi: 10.3389/fendo.2022.1028616. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36419768 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical