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CMTM1_v17 is a novel potential therapeutic target in breast cancer.
- Source :
-
Oncology reports [Oncol Rep] 2014 Nov; Vol. 32 (5), pp. 1829-36. Date of Electronic Publication: 2014 Aug 20. - Publication Year :
- 2014
-
Abstract
- Chemokine-like factor (CKLF)-like MARVEL transmembrane domain-containing 1 (CMTM1) consists of at least 23 alternatively spliced isoforms designated CMTM1_v1-v23. In the present study, we detected CMTM1_v17 expression in multiple human normal and tumor tissues and found that CMTM1_v17 was highly expressed in testis and many tumor tissues including breast tumor. The overexpression of CMTM1_v17 in the breast cancer cell line MDA-MB-231 promoted cell proliferation and resistance to tumor necrosis factor-α (TNF-α)-induced apoptosis. Moreover, siRNA-mediated silencing of CMTM1_v17 sensitized MDA-MB-231 cells to TNF-α-induced apoptosis. We propose that CMTM1_v17 may be a novel potential target for therapy in breast cancer patients. The present study provides insight into a novel mechanism by which CMTM1_v17 enhances cellular proliferation and abrogates TNF-α-induced apoptosis. These findings also have implications for clinical practice as they highlight the potential for therapeutic targeting of CMTM1_v17 for the treatment of breast and other cancers in which CMTM1_v17 impacts cellular proliferation and survival.
- Subjects :
- Apoptosis
Breast Neoplasms drug therapy
Breast Neoplasms genetics
Breast Neoplasms metabolism
Cell Line, Tumor
Cell Proliferation
Chemokines genetics
Female
HEK293 Cells
HeLa Cells
Hep G2 Cells
Humans
MARVEL Domain-Containing Proteins genetics
MCF-7 Cells
Male
Protein Isoforms genetics
Protein Isoforms metabolism
Testicular Neoplasms metabolism
Testicular Neoplasms pathology
Tumor Necrosis Factor-alpha pharmacology
Antineoplastic Agents pharmacology
Breast Neoplasms pathology
Chemokines antagonists & inhibitors
Chemokines metabolism
MARVEL Domain-Containing Proteins antagonists & inhibitors
MARVEL Domain-Containing Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1791-2431
- Volume :
- 32
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Oncology reports
- Publication Type :
- Academic Journal
- Accession number :
- 25175386
- Full Text :
- https://doi.org/10.3892/or.2014.3429