scispace - formally typeset
A

Adrian Biddle

Researcher at Queen Mary University of London

Publications -  30
Citations -  1776

Adrian Biddle is an academic researcher from Queen Mary University of London. The author has contributed to research in topics: Cancer stem cell & Cancer. The author has an hindex of 17, co-authored 23 publications receiving 1522 citations. Previous affiliations of Adrian Biddle include Wellcome Trust/Cancer Research UK Gurdon Institute & Dartmouth College.

Papers
More filters
Journal ArticleDOI

Cancer Stem Cells in Squamous Cell Carcinoma Switch between Two Distinct Phenotypes That Are Preferentially Migratory or Proliferative

TL;DR: A need to define therapeutic targets that can eradicate both EMT and self-renewing CSC variants to achieve effective SCC treatment is suggested.
Journal ArticleDOI

Hybrid epithelial/mesenchymal phenotypes promote metastasis and therapy resistance across carcinomas.

TL;DR: Together, these studies drive the emerging notion that cells in a hybrid E/M phenotype may occupy ‘metastatic sweet spot’ in multiple subtypes of carcinomas, and pathways linked to this hybrids may be relevant as prognostic biomarkers as well as a promising therapeutic targets.
Journal ArticleDOI

Cancer stem cells and EMT in carcinoma

TL;DR: Cancer stem cells and their link with EMT are reviewed, and the importance of this link in metastasis and therapeutic resistance of tumours is explored, and new evidence from the laboratory demonstrating that cancer stem cells display a remarkable phenotypic plasticity that enables them to switch between an epithelial phenotype that drives tumour growth and an EMT phenotype that drove metastasis is discussed.
Journal ArticleDOI

Normal and malignant epithelial cells with stem-like properties have an extended G2 cell cycle phase that is associated with apoptotic resistance

TL;DR: These data indicate that both normal and malignant human epithelial cells with stem-like properties show greater resistance to apoptosis associated with extended G2 cell cycle phase, and that this property is not a consequence of neoplastic transformation.