In this paper, Prox1 is presented as a tumor-suppressive regulator in breast cancer that suppresses proliferation, migration, and the Warburg effect. The abstract also states that its anti-tumor effect is mediated by direct repression of c-Myc transcription.
First-pass extracted concept
Prox1
Aliases
PROX1
Extracted Explainers
What the tool is doing
What problem it solves
Evidence Snippets
Supporting Sources
Linked Claims
Prox1 over-expression suppresses proliferation, migration, and the Warburg effect in human breast cancer cells without inducing apoptosis.
Breast tumors from human patients exhibited reduced Prox1 expression, and higher Prox1 expression was associated with favorable prognosis in breast cancer patients.
Prox1 is a negative regulator of proliferation and tumor-related metabolism in breast cancer.
Prox1 over-expression inhibits breast tumor growth in heterotopic and orthotopic xenograft mouse models.
The anti-tumorigenic effect of Prox1 is mediated by direct repression of c-Myc transcription and its downstream target genes.
c-Myc over-expression from an artificial promoter not targeted by Prox1 reverses Prox1 anti-tumor effects.
Prox1 is suggested as a promising therapeutic gene for breast cancer.