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Hair follicle regeneration suppresses Ras-driven oncogenic growth.

Cristiana M Pineda | David G Gonzalez | Catherine Matte-Martone | Jonathan Boucher | Elizabeth Lathrop | Sara Gallini | Nathan R Fons | Tianchi Xin | Karen Tai | Edward Marsh | Don X Nguyen | Kathleen C Suozzi | Slobodan Beronja | Valentina Greco
The Journal of cell biology | 2019

Mutations associated with tumor development in certain tissues can be nontumorigenic in others, yet the mechanisms underlying these different outcomes remains poorly understood. To address this, we targeted an activating Hras mutation to hair follicle stem cells and discovered that Hras mutant cells outcompete wild-type neighbors yet are integrated into clinically normal skin hair follicles. In contrast, targeting the Hras mutation to the upper noncycling region of the skin epithelium leads to benign outgrowths. Follicular Hras mutant cells autonomously and nonautonomously enhance regeneration, which directs mutant cells into continuous tissue cycling to promote integration rather than aberrancy. This follicular tolerance is maintained under additional challenges that promote tumorigenesis in the epidermis, including aging, injury, and a secondary mutation. Thus, the hair follicle possesses a unique, enhanced capacity to integrate and contain Hras mutant cells within both homeostatic and perturbed tissue, demonstrating that in the skin, multiple, distinct mechanisms exist to suppress oncogenic growth.

Pubmed ID: 31488583

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR001863
  • Agency: NCI NIH HHS, United States
    Id: F31 CA206419
  • Agency: NIAMS NIH HHS, United States
    Id: R01 AR072668
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM007499
  • Agency: NCI NIH HHS, United States
    Id: R01 CA191489
  • Agency: NIAMS NIH HHS, United States
    Id: R01 AR063663
  • Agency: NIAMS NIH HHS, United States
    Id: R01 AR067755

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