4.7 Article

The functions and molecular mechanisms of Tribbles homolog 3 (TRIB3) implicated in the pathophysiology of cancer

Journal

INTERNATIONAL IMMUNOPHARMACOLOGY
Volume 114, Issue -, Pages -

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ELSEVIER
DOI: 10.1016/j.intimp.2022.109581

Keywords

Cancer; TRIB3; Signal transduction; Chemoresistance

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Currently, cancer is the second leading cause of death worldwide, and the burden of cancer continues to increase. Understanding the molecular pathways involved in cancer initiation and development may lead to new treatments. Recent research suggests that TRIB3 plays a significant role in oncogenesis in various types of cancer.
Currently, cancer ranks as the second leading cause of death worldwide, and at the same time, the burden of cancer continues to increase. The underlying molecular pathways involved in the initiation and development of cancer are the subject of considerable research worldwide. Further understanding of these pathways may lead to new cancer treatments. Growing data suggest that Tribble's homolog 3 (TRIB3) is essential in oncogenesis in many types of cancer. The mammalian tribbles family's proteins regulate various cellular and physiological functions, such as the cell cycle, stress response, signal transduction, propagation, development, differentiation, immunity, inflammatory processes, and metabolism. To exert their activities, Tribbles proteins must alter key signaling pathways, including the mitogen-activated protein kinase (MAPK) and phosphatidylinositol 3 kinase (PI3K)/AKT pathways. Recent evidence supports that TRIB3 dysregulation has been linked to various diseases, including tumor development and chemoresistance. It has been speculated that TRIB3 may either promote or inhibit the onset and development of cancer. However, it is still unclear how TRIB3 performs this dual function in cancer. In this review, we present and discuss the most recent data on the role of TRIB3 in cancer pathophysi-ology and chemoresistance. Furthermore, we describe in detail the molecular mechanism TRIB3 regulates in cancer.

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