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Overcoming anoikis – pathways to anchorage-independent growth in cancer

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TLDR
A better understanding of the mechanisms underlying anoikis resistance could help to counteract tumor progression and prevent metastasis formation, which is one of the hallmarks of cancer cells.
Abstract
Anoikis (or cell-detachment-induced apoptosis) is a self-defense strategy that organisms use to eliminate 'misplaced' cells, i.e. cells that are in an inappropriate location. Occasionally, detached or misplaced cells can overcome anoikis and survive for a certain period of time in the absence of the correct signals from the extracellular matrix (ECM). If cells are able to adapt to their new environment, then they have probably become anchorage-independent, which is one of the hallmarks of cancer cells. Anoikis resistance and anchorage-independency allow tumor cells to expand and invade adjacent tissues, and to disseminate through the body, giving rise to metastasis. Thus, overcoming anoikis is a crucial step in a series of changes that a tumor cell undergoes during malignant transformation. Tumor cells have developed a variety of strategies to bypass or overcome anoikis. Some strategies consist of adaptive cellular changes that allow the cells to behave as they would in the correct environment, so that induction of anoikis is aborted. Other strategies aim to counteract the negative effects of anoikis induction by hyperactivating survival and proliferative cascades. The recently discovered processes of autophagy and entosis also highlight the contribution of these mechanisms to rendering the cells in a dormant state until they receive a signal initiated at the ECM, thereby circumventing anoikis. In all situations, the final outcome is the ability of the tumor to grow and metastasize. A better understanding of the mechanisms underlying anoikis resistance could help to counteract tumor progression and prevent metastasis formation.

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Journal ArticleDOI

Apoptosis, autophagy, necroptosis, and cancer metastasis

TL;DR: This review summarizes the recent advances in the understanding of the mechanisms by which key regulators of apoptosis, autophagy, and necroptosis participate in cancer metastasis and discusses the crosstalk between apoptosis-autophagy-and-novoptosis involved in the regulation of cancer metastatic processes.
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The Roles of Autophagy in Cancer

TL;DR: The mechanism of autophagy under stressful conditions and its roles in tumor suppression and promotion in cancer and in cancer stem-cells are summarized and how Autophagy is a promising potential therapeutic target in cancer treatment is discussed.
Journal Article

A non-apoptotic cell death process, entosis, that occurs by cell-in-cell invasion.

TL;DR: In this paper, the authors describe a non-apoptotic cell death program in matrix-detached cells, termed entosis, that is initiated by a previously unrecognized and unusual process involving the invasion of one cell into another, leading to a transient state in which a live cell is contained within a neighboring host cell.
References
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Journal ArticleDOI

The absence of caveolin-1 increases proliferation and anchorage- independent growth by a Rac-dependent, Erk-independent mechanism.

TL;DR: Insight is provided into the mechanisms regulating growth of cancer cells, which frequently lose Cav1 function and Anchorage independence and increased proliferation in Cav1-deficient tumoral and null cells are thus due to an increased fraction of active Rac1 at membrane ordered domains.
Journal ArticleDOI

Hydrogen peroxide inhibits non-small cell lung cancer cell anoikis through the inhibition of caveolin-1 degradation

TL;DR: It is reported here that Cav-1 plays a key role as a negative regulator of anoikis through a reactive oxygen species (ROS)-dependent mechanism in human lung carcinoma H460 cells, and a novel role of hydrogen peroxide as an endogenous suppressor of cell ano Kikis through its stabilizing effect on Cav- 1 is indicated.
Journal ArticleDOI

p66Shc mediates anoikis through RhoA

TL;DR: In this article, the constitutive form of the adapter Shc, p52Shc, confers survival properties, whereas the longer p66Shc signals death through association with cytochrome c. This pathway stimulates the formation of focal adhesions and stress fibers in attached cells and tensiondependent cell death upon detachment.
Journal ArticleDOI

CAV1 inhibits metastatic potential in melanomas through suppression of the integrin/Src/FAK signaling pathway.

TL;DR: Experimental evidence is provided that CAV1 may function as an antimetastatic gene in malignant melanoma, by using B16F10 melanoma cells as an experimental system.
Book ChapterDOI

Mitochondrial protein quality control systems in aging and disease.

TL;DR: The current knowledge of cellular quality control systems is summarized with special emphasis on the role of the mitochondrial PQC system and its impact on biological aging and disease.
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Trending Questions (1)
Do cells that metastasize follow anchorage dependence?

Anoikis resistance and anchorage-independency allow tumor cells to expand and invade adjacent tissues, and to disseminate through the body, giving rise to metastasis.