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LKB1/STK11 inactivation leads to expansion of a prometastatic tumor subpopulation in melanoma.

Wenjin Liu | Kimberly B Monahan | Adam D Pfefferle | Takeshi Shimamura | Jessica Sorrentino | Keefe T Chan | David W Roadcap | David W Ollila | Nancy E Thomas | Diego H Castrillon | C Ryan Miller | Charles M Perou | Kwok-Kin Wong | James E Bear | Norman E Sharpless
Cancer cell | 2012

Germline mutations in LKB1 (STK11) are associated with the Peutz-Jeghers syndrome (PJS), which includes aberrant mucocutaneous pigmentation, and somatic LKB1 mutations occur in 10% of cutaneous melanoma. By somatically inactivating Lkb1 with K-Ras activation (±p53 loss) in murine melanocytes, we observed variably pigmented and highly metastatic melanoma with 100% penetrance. LKB1 deficiency resulted in increased phosphorylation of the SRC family kinase (SFK) YES, increased expression of WNT target genes, and expansion of a CD24(+) cell population, which showed increased metastatic behavior in vitro and in vivo relative to isogenic CD24(-) cells. These results suggest that LKB1 inactivation in the context of RAS activation facilitates metastasis by inducing an SFK-dependent expansion of a prometastatic, CD24(+) tumor subpopulation.

Pubmed ID: 22698401

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: R01 CA122794
  • Agency: NCI NIH HHS, United States
    Id: R01 CA137181
  • Agency: NCI NIH HHS, United States
    Id: R01 CA166480
  • Agency: NCI NIH HHS, United States
    Id: R01 CA140594
  • Agency: NIEHS NIH HHS, United States
    Id: T32 ES007126
  • Agency: NCI NIH HHS, United States
    Id: P30 CA016086
  • Agency: NCI NIH HHS, United States
    Id: P01 CA154303
  • Agency: NCI NIH HHS, United States
    Id: R01 CA163896

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In vivo imaging software which facilitates workflow for in vivo optical, X-ray and microCT image acquisition, analysis and data organization.

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