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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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Loss of DOK2 induces carboplatin resistance in ovarian cancer via suppression of apoptosis

TL;DR: A screening methodology that analyzes the epigenome and informatically identifies candidate genes followed by in vitro culture screening of the candidate genes showed that loss of DOK2 induces chemotherapy resistance by decreasing the level of apoptosis in response to treatment.
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αB-crystallin: Portrait of a malignant chaperone as a cancer therapeutic target.

TL;DR: This review will focus on new insights into the molecular mechanisms by which oncogenes, oxidative stress, matrix detachment and other tumor microenvironmental stressors deregulate αB-crystallin expression and evaluate emerging strategies to therapeutically target and/or interacting proteins to selectively activate apoptotic cell death machinery in an effort to improve outcomes for patients with metastatic disease.
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STIM1 is a metabolic checkpoint regulating the invasion and metastasis of hepatocellular carcinoma.

TL;DR: The data provide the molecular basis that STIM1 orchestrates invasion and metastasis via reprogramming HCC metabolism and shift the anabolic/catabolic balance, i.e., from aerobic glycolysis towards AMPK-activated fatty acid oxidation (FAO), which contributed to Snail1-driven metastasis and anoikis-resistance.
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Regulation of anoikis by deleted in breast cancer-1 (DBC1) through NF-κB

TL;DR: The results indicate that DBC1 is an important co-factor for the control of the IKK-β-NF-κB signaling pathway that regulates anoikis, and correlates with a poorer prognosis in some cases.
References
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Related Papers (5)
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.