scispace - formally typeset
Open AccessJournal ArticleDOI

Overcoming anoikis – pathways to anchorage-independent growth in cancer

Reads0
Chats0
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.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Targeting tumor multicellular aggregation through IGPR-1 inhibits colon cancer growth and improves chemotherapy

TL;DR: It is demonstrated that expression of immunoglobulin containing and proline-rich receptor-1 (IGPR-1) is upregulated in human primary colon cancer, and interfering with its adhesive function inhibits multicellular aggregation and, increases cell death.
Journal ArticleDOI

DANGER is involved in high glucose-induced radioresistance through inhibiting DAPK-mediated anoikis in non-small cell lung cancer

TL;DR: Evidence is offered that overexpression of DANGER and the subsequent inhibitory effect on DAPK kinase activity are critical responses that account for HG-induced radioresistance of NSCLC.
Journal ArticleDOI

Consecutive entosis stages in human substrate-dependent cultured cells.

TL;DR: In substrate-dependent cultures, entosis requires microfilaments, microtubules and the Golgi complex for cell invasion, but not for internalized cell degradation, so it is demonstrated that actin filaments in the entotic as well as invading cells were crucial for entosis.
Journal ArticleDOI

EphB6 promotes anoikis by modulating EphA2 signaling

TL;DR: The findings implicate EphB6 as a negative regulator of EphA2 oncogenic signaling, which is frequently silenced in invasive and metastatic cancers, and promotes anoikis resistance in MCF7 breast cancer cells.
Journal ArticleDOI

Evaluation of MicroRNAs Regulating Anoikis Pathways and Its Therapeutic Potential

TL;DR: This review will be examining miRNAs that have been found to promote anoikis sensitivity in numerous cancer types followed by miRN as well as major signaling pathways involved in the action of the each of these miRNA to gain a better understanding on how mi RNAs regulate anoika.
References
More filters
Journal ArticleDOI

Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation

TL;DR: It is proposed that the metabolism of cancer cells, and indeed all proliferating cells, is adapted to facilitate the uptake and incorporation of nutrients into the biomass needed to produce a new cell.
Journal ArticleDOI

Epithelial-mesenchymal transition and its implications for fibrosis.

TL;DR: This review highlights recent advances in the process of EMT signaling in health and disease and how it may be attenuated or reversed by selective cytokines and growth factors.
Journal ArticleDOI

Cellular response to oxidative stress: signaling for suicide and survival.

TL;DR: The various signaling pathways known to be activated in response to oxidative stress in mammalian cells, the mechanisms leading to their activation, and their roles in influencing cell survival are discussed.
Journal ArticleDOI

NF-κB activation by tumour necrosis factor requires the Akt serine–threonine kinase

TL;DR: It is shown that the Akt serine–threonine kinase is involved in the activation of NF-κB by tumour necrosis factor (TNF), and that Akt is part of a signalling pathway that is necessary for inducing key immune and inflammatory responses.
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.