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Wake Forest University

SOX7 is downregulated and functions as a tumor suppressive transcription factor in breast cancer

Abstract

dc:description.abstract

Second only to lung cancer, breast cancer is the leading cause of cancer-related deaths in American women. Breast cancer is a heterogeneous set of diseases characterized by aberrant genetic and epigenetic states, often leading to the ablation of tumor suppressors. Loss of tumor suppressor function has been established as a driver of disease progression in breast cancer patients. Thus, understanding the deregulation of tumor suppressor activity may lead to the identification of potential therapeutic targets whose inhibition can restore tumor suppressor function and, consequently, an anti-proliferative cellular state.

Degree

thesis:*
Grantor dc:publisher
Wake Forest University
Year dc:date.issued
2014

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Stovall, Daniel B.

Subjects

dc:subject × 1

Rights

Language dc:language.iso
en

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/10339/39287
OAI identifier oai:identifier
oai:wakespace.lib.wfu.edu:10339/39287

Chain of custody

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Harvested from
Wake Forest University
Base URL
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Last updated
2026-07-27
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citation

Stovall, Daniel B.. SOX7 is downregulated and functions as a tumor suppressive transcription factor in breast cancer. Wake Forest University, 2014. http://hdl.handle.net/10339/39287