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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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Mitochondrial clearance by the STK38 kinase supports oncogenic Ras-induced cell transformation.

TL;DR: Critical roles of the STK38 protein kinase in oncogenic Ras transformation are reported and novel molecular players that determine whether Ras-transformed human cells die or survive upon cell detachment are revealed, which could be exploited for the development of novel strategies to target Ras- transformed cells.
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WIP promotes in-vitro invasion ability, anchorage independent growth and EMT progression of A549 lung adenocarcinoma cells by regulating RhoA levels.

TL;DR: It is found that the expression of WIP was significantly upregulated in metastatic A5-RT3 cells compared to its parental non-tumorigenic HaCaT cells, indicating that WIP might be executing its function by regulating RhoA.
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Synthetic Molecules that Protect Cells from Anoikis and Their Use in Cell Transplantation

TL;DR: Molecular biological analysis indicates that water-soluble molecules bind to and induce clusters of integrins and heparan-sulfate-bound syndecans, two classes of receptors that are important for extracellular matrix-mediated cell survival, and may provide a starting point for the design of new synthetic tools for cell-based therapy.
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miR-429 inhibits metastasis by targeting KIAA0101 in Soft Tissue Sarcoma

TL;DR: It is demonstrated miR‐429 mediates deregulation of KIAA0101 by acting as an anti‐metastatic miRNA that targets KIAa0101 pro‐ Metastatic gene during metastasis of STS.
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Proteomic and transcriptomic profiling identifies mediators of anchorage-independent growth and roles of inhibitor of differentiation proteins in invasive lobular carcinoma

TL;DR: A comprehensive study of anchorage independence in human ILC cell lines provides mechanistic insights and clinical implications for metastatic dissemination of ILC and implicates ID1 and ID3 as novel drivers and therapeutic targets for lobular breast cancer.
References
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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.