TY - JOUR
T1 - The dark side of SOX2
T2 - Cancer - A comprehensive overview
AU - Wuebben, Erin L.
AU - Rizzino, Angie
N1 - Funding Information:
Phillip Wilder is thanked for reading this review and providing helpful comments. Research in this laboratory was supported in part by grants from the Nebraska Department of Health and Human Services (2016-42 and Stem Cell 2015-01), the Pediatric Cancer Research Program, the Regenerative Medicine Program and the Fred & Pamela Buffett Cancer Center. Core facilities used by this laboratory were supported in part by a Cancer Center Support Grant from the National Cancer Institute (P30CA036727).
Publisher Copyright:
© Wuebben et al.
PY - 2017
Y1 - 2017
N2 - The pluripotency-associated transcription factor SOX2 is essential during mammalian embryogenesis and later in life, but SOX2 expression can also be highly detrimental. Over the past 10 years, SOX2 has been shown to be expressed in at least 25 different cancers. This review provides a comprehensive overview of the roles of SOX2 in cancer and focuses on two broad topics. The first delves into the expression and function of SOX2 in cancer focusing on the connection between SOX2 levels and tumor grade as well as patient survival. As part of this discussion, we address the developing connection between SOX2 expression and tumor drug resistance. We also call attention to an under-appreciated property of SOX2, its levels in actively proliferating tumor cells appear to be optimized to maximize tumor growth - too little or too much SOX2 dramatically alters tumor growth. The second topic of this review focuses on the exquisite array of molecular mechanisms that control the expression and transcriptional activity of SOX2. In addition to its complex regulation at the transcriptional level, SOX2 expression and activity are controlled carefully by microRNAs, long non-coding RNAs, and post-translational modifications. In the Conclusion and Future Perspectives section, we point out that there are still important unanswered questions. Addressing these questions is expected to lead to new insights into the functions of SOX2 in cancer, which will help design novels strategies for more effectively treating some of the most deadly cancers.
AB - The pluripotency-associated transcription factor SOX2 is essential during mammalian embryogenesis and later in life, but SOX2 expression can also be highly detrimental. Over the past 10 years, SOX2 has been shown to be expressed in at least 25 different cancers. This review provides a comprehensive overview of the roles of SOX2 in cancer and focuses on two broad topics. The first delves into the expression and function of SOX2 in cancer focusing on the connection between SOX2 levels and tumor grade as well as patient survival. As part of this discussion, we address the developing connection between SOX2 expression and tumor drug resistance. We also call attention to an under-appreciated property of SOX2, its levels in actively proliferating tumor cells appear to be optimized to maximize tumor growth - too little or too much SOX2 dramatically alters tumor growth. The second topic of this review focuses on the exquisite array of molecular mechanisms that control the expression and transcriptional activity of SOX2. In addition to its complex regulation at the transcriptional level, SOX2 expression and activity are controlled carefully by microRNAs, long non-coding RNAs, and post-translational modifications. In the Conclusion and Future Perspectives section, we point out that there are still important unanswered questions. Addressing these questions is expected to lead to new insights into the functions of SOX2 in cancer, which will help design novels strategies for more effectively treating some of the most deadly cancers.
KW - Cancer
KW - Cancer stem cell markers
KW - SOX2
KW - Tumor progression
KW - Tumor-initiating cells
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U2 - 10.18632/oncotarget.16570
DO - 10.18632/oncotarget.16570
M3 - Review article
C2 - 28388544
AN - SCOPUS:85021828163
SN - 1949-2553
VL - 8
SP - 44917
EP - 44943
JO - Oncotarget
JF - Oncotarget
IS - 27
ER -