4.8 Review

Mechanisms and context underlying the role of autophagy in cancer metastasis

Journal

AUTOPHAGY
Volume 14, Issue 7, Pages 1110-1128

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/15548627.2018.1450020

Keywords

anoikis; autophagy; epithelial-mesenchymal transition; extracellular matrix; fibrosis; focal adhesion; integrin; metastasis; tumor microenvironment

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Funding

  1. Lois High Berstler Research Endowment Fund
  2. Four Diamonds Fund of the Pennsylvania State University College of Medicine

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Macroautophagy/autophagy is a fundamental cellular degradation mechanism that maintains cell homeostasis, regulates cell signaling, and promotes cell survival. Its role in promoting tumor cell survival in stress conditions is well characterized, and makes autophagy an attractive target for cancer therapy. Emerging research indicates that autophagy also influences cancer metastasis, which is the primary cause of cancer-associated mortality. However, data demonstrate that the regulatory role of autophagy in metastasis is multifaceted, and includes both metastasis-suppressing and -promoting functions. The metastasis-suppressing functions of autophagy, in particular, have important implications for autophagy-based treatments, as inhibition of autophagy may increase the risk of metastasis. In this review, we discuss the mechanisms and context underlying the role of autophagy in metastasis, which include autophagy-mediated regulation of focal adhesion dynamics, integrin signaling and trafficking, Rho GTPase-mediated cytoskeleton remodeling, anoikis resistance, extracellular matrix remodeling, epithelial-to-mesenchymal transition signaling, and tumor-stromal cell interactions. Through this, we aim to clarify the context-dependent nature of autophagy-mediated metastasis and provide direction for further research investigating the role of autophagy in cancer metastasis.

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