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Inhibiting the SUMO Pathway Represses the Cancer Stem Cell Population in Breast and Colorectal Carcinomas.
- Source :
-
Stem cell reports [Stem Cell Reports] 2016 Dec 13; Vol. 7 (6), pp. 1140-1151. Date of Electronic Publication: 2016 Dec 01. - Publication Year :
- 2016
-
Abstract
- Many solid cancers have an expanded CD44 <superscript>+/hi</superscript> /CD24 <superscript>-/low</superscript> cancer stem cell (CSC) population, which are relatively chemoresistant and drive recurrence and metastasis. Achieving a more durable response requires the development of therapies that specifically target CSCs. Recent evidence indicated that inhibiting the SUMO pathway repressed tumor growth and invasiveness, although the mechanism has yet to be clarified. Here, we demonstrate that inhibition of the SUMO pathway repressed MMP14 and CD44 with a concomitant reduction in cell invasiveness and functional loss of CSCs in basal breast cancer. Similar effects were demonstrated with a panel of E1 and E3 SUMO inhibitors. Identical results were obtained in a colorectal cancer cell line and primary colon cancer cells. In both breast and colon cancer, SUMO-unconjugated TFAP2A mediated the effects of SUMO inhibition. These data support the development of SUMO inhibitors as an approach to specifically target the CSC population in breast and colorectal cancer.<br /> (Copyright © 2016 The Author(s). Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Anacardic Acids chemistry
Anacardic Acids pharmacology
Breast Neoplasms metabolism
Carcinogenesis drug effects
Carcinogenesis metabolism
Carcinogenesis pathology
Cell Line, Tumor
Colorectal Neoplasms metabolism
Female
Gene Knockdown Techniques
Humans
Hyaluronan Receptors metabolism
Matrix Metalloproteinase 14 metabolism
Neoplasm Invasiveness
Neoplastic Stem Cells drug effects
Phenotype
Xenograft Model Antitumor Assays
Breast Neoplasms pathology
Colorectal Neoplasms pathology
Neoplastic Stem Cells metabolism
Neoplastic Stem Cells pathology
Signal Transduction drug effects
Small Ubiquitin-Related Modifier Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2213-6711
- Volume :
- 7
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Stem cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 27916539
- Full Text :
- https://doi.org/10.1016/j.stemcr.2016.11.001