Cell adhesion molecules and their relation to (cancer) cell stemness

Ensieh Farahani1, Hirak K Patra, Jaganmohan R Jangamreddy

  • 1Department of Clinical and Experimental Medicine, Division of Cell Biology and Integrative Regenerative Medicine Center (IGEN) and.

Carcinogenesis
|February 18, 2014
PubMed

Insights

This review compares cell reprogramming and carcinogenesis, highlighting how adhesion molecules influence cancer stem cells (CSCs) division and metastasis. Targeting these molecules offers new anticancer drug strategies for solid tumors.

Area of Science:

  • Oncology and Cell Biology
  • Molecular Mechanisms of Cancer

Background:

  • Solid tumors, particularly in advanced metastatic stages, remain largely incurable despite extensive research.
  • Cancer stem cells (CSCs) are crucial drivers of tumor growth, metastasis, and therapeutic resistance.
  • Adhesion molecules play a fundamental role in normal stem cell (SC) biology and are implicated in cancer progression.

Purpose of the Study:

  • To compare the processes of cellular reprogramming and carcinogenesis.
  • To elucidate the role of adhesion molecules in regulating cancer stem cell (CSC) behavior, including division and interaction with the extracellular matrix.
  • To analyze changes in adhesion molecule expression during cancer progression and metastasis.

Main Methods:

  • Review of existing literature comparing stem cells (SCs) and cancer stem cells (CSCs).
  • Analysis of the role of adhesion molecules (e.g., cadherins, integrins) and transcription factors (e.g., Twist, Snail) in cancer progression.
  • Discussion of CSC-targeting strategies involving adhesion molecules and tumor vasculature.

Main Results:

  • Adhesion molecules significantly influence CSC division (symmetric/asymmetric) and their interactions with the extracellular matrix.
  • Expression patterns of key adhesion molecules and transcription factors change as cancer progresses and metastases develop.
  • These molecular changes are critical for epithelial-to-mesenchymal transition (EMT) and anoikis evasion.

Conclusions:

  • Understanding the interplay between adhesion molecules and CSCs provides insights into carcinogenesis and metastasis.
  • Adhesion molecules are critical regulators of CSC behavior and represent promising targets for novel anticancer therapies.
  • Targeting CSCs via adhesion molecules or tumor vasculature offers new therapeutic avenues for intractable solid tumors.

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