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Chemotaxis in cancer

TLDR
This Review summarizes how chemotaxis directs the different behaviours of tumour cells and stromal cells in vivo, how molecular pathways regulateChemotaxis in tumours and how chemtaxis choreographs cell behaviour to shape the tumour microenvironment and to determine metastatic spread.
Abstract
Chemotaxis of tumour cells and stromal cells in the surrounding microenvironment is an essential component of tumour dissemination during progression and metastasis. This Review summarizes how chemotaxis directs the different behaviours of tumour cells and stromal cells in vivo, how molecular pathways regulate chemotaxis in tumour cells and how chemotaxis choreographs cell behaviour to shape the tumour microenvironment and to determine metastatic spread. The central importance of chemotaxis in cancer progression is highlighted by discussion of the use of chemotaxis as a prognostic marker, a treatment end point and a target of therapeutic intervention.

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Cancer Invasion and the Microenvironment: Plasticity and Reciprocity

TL;DR: The cell-matrix and cell-cell adhesion, protease, and cytokine systems that underlie tissue invasion by cancer cells are described and explained to explain how the reciprocal reprogramming of both the tumor cells and the surrounding tissue structures not only guides invasion, but also generates diverse modes of dissemination.
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Classifying collective cancer cell invasion

TL;DR: A framework for addressing potential mechanisms, experimental strategies and technical challenges to study collective cancer cell invasion is proposed.
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Three-dimensional microfluidic model for tumor cell intravasation and endothelial barrier function

TL;DR: Evidence is provided that the endothelium poses a barrier to tumor cell intravasation that can be regulated by factors present in the tumor microenvironment.
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Differential macrophage programming in the tumor microenvironment.

TL;DR: Targeting molecular pathways regulating TAM polarization holds great promise for anticancer therapy.
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Crossing the endothelial barrier during metastasis

TL;DR: How cancer cells cross the endothelial barrier during extravasation is described and how different receptors, signalling pathways and circulating cells such as leukocytes and platelets contribute to this process are described.
References
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Journal ArticleDOI

PI 3-Kinases and PTEN: How Opposites Chemoattract

TL;DR: Two recent reports examine how the metabolism of these lipids by phosphatidylinositol 3-kinases and the PTEN 3-phosphoinositide phosphatase may coordinate G protein coupled signaling pathways during eukaryotic chemotaxis.
Journal ArticleDOI

Regulator of G-protein signaling (RGS) proteins in cancer biology

TL;DR: This review highlights recent studies detailing changes in RGS transcript expression during oncogenesis, single nucleotide polymorphisms in R GS proteins linked to lung and bladder cancers, and specific roles for RGS proteins in multiple cancer types.
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CSF‐1 and its receptor in breast carcinomas and neoplasms of the female reproductive tract

TL;DR: CSF‐1 and its receptor have been more recently shown to be expressed by carcinomas of the breast and other epithelia of the female reproductive tract where activation of the receptor by ligand produced by the tumor cells or by stromal elements stimulates tumor cell invasion by a urokinase‐dependent mechanism.
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Regulation of the cytoskeleton by Rho-family GTPases: implications for tumour cell invasion.

TL;DR: The balance of Rac and Rho activities and intracellular localization appears to be critical in determining the cellular phenotype.
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What part of chemotaxis in cancer has not been studied yet?

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What part of chemotaxis in breast cancer has not been studied yet?

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