Differences in gynecologic tumor development in Amhr2-Cre mice with KRAS G12D or KRAS G12V mutations

How different KRAS variants impact tumor initiation and progression in vivo has not been thoroughly examined. We hypothesize that the ability of either KRAS or KRAS mutations to initiate tumor formation is context dependent. Amhr2-Cre mice express Cre recombinase in tissues that develop into the fal...

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Bibliographic Details
Published in:Scientific reports 2020-11, Vol.10 (1), p.20678
Main Authors: Kun, Eucharist H S, Tsang, Yvonne T M, Lin, Sophia, Pan, Sophia, Medapalli, Tejas, Malpica, Anais, Richards, JoAnne S, Gershenson, David M, Wong, Kwong-Kwok
Format: Article
Language:English
Subjects:
Animals
Female
Genital Neoplasms, Female - genetics
Genotype
Granulosa Cell Tumor - genetics
Humans
Integrases - genetics
Leiomyoma - genetics
Leiomyosarcoma - genetics
Mice
Mice, Inbred C57BL
Mutation - genetics
Proto-Oncogene Proteins p21(ras) - genetics
PTEN Phosphohydrolase - genetics
Signal Transduction - genetics
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Summary:How different KRAS variants impact tumor initiation and progression in vivo has not been thoroughly examined. We hypothesize that the ability of either KRAS or KRAS mutations to initiate tumor formation is context dependent. Amhr2-Cre mice express Cre recombinase in tissues that develop into the fallopian tubes, uterus, and ovaries. We used these mice to conditionally express either the KRAS or KRAS mutation. Mice with the genotype Amhr2-Cre Pten Kras (G12D mice) had abnormal follicle structures and developed low-grade serous ovarian carcinomas with 100% penetrance within 18 weeks. In contrast, mice with the genotype Amhr2-Cre Pten Kras (G12V mice) had normal follicle structures, and about 90% of them developed uterine tumors with diverse histological features resembling those of leiomyoma and leiomyosarcoma. Granulosa cell tumors also developed in G12V mice. Differences in cell-signaling pathways in the uterine tissues of G12D and G12V mice were identified using RNA sequencing and reverse-phase protein array analyses. We found that CTNNB1, IL1A, IL1B, TNF, TGFB1, APP, and IL6 had the higher activity in G12V mice than in G12D mice. These mouse models will be useful for studying the differences in signaling pathways driven by Kras or Kras mutations to aid development of targeted therapies for specific KRAS mutant variants. Our leiomyoma model driven by the Kras mutation will also be useful in deciphering the malignant progression from leiomyoma to leiomyosarcoma.
ISSN:2045-2322