From autonomy to community; new perspectives on tumorigenicity and therapy resistance

Cancer Treat Rev. 2015 Dec;41(10):809-13. doi: 10.1016/j.ctrv.2015.10.004. Epub 2015 Oct 20.

Abstract

Subclones of cancer cells evading treatment represent the major challenge in oncology. Despite recent advances, tumors not responding to treatments are still a severe risk to cancer patients, and oncologists have, as of now, little effective therapy to offer patients with systemic cancer disease. The widely discussed cancer stem cell (CSC) paradigm was originally launched as an explanation to the existence of small cell populations resistant to therapy within the heterogeneous tumor, but has so far unfortunately, offered little concrete improvement in cancer treatment regimes. The launch of the CSC hypothesis did, however, highlight the significance of therapy targeting specific tumor-driving processes, and even more importantly, an increased awareness of a phenomenon well known to stem cell researchers; non-genetic phenotypic heterogeneity of cells with common origin. Here, the scientific background of the CSC theory is revisited and the evidence for CSCs is discussed, along with the importance of considering CSC's dependency of their habitat for survival and growth. Furthermore, recent advances in cancer cell heterogeneity and new possibilities for studying therapy responses in cell clones within the natural tumor environment using patient derived xenograft (PDX) models, are reviewed.

Keywords: Cancer stem cell; Hypothesis; Intratumor heterogeneity; PDX; Tumorigenicity; Xenografts.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Carcinogenesis*
  • Drug Resistance, Neoplasm*
  • Humans
  • Neoplasm Transplantation
  • Neoplasms / drug therapy*
  • Neoplastic Stem Cells*
  • Xenograft Model Antitumor Assays