期刊
CANCER BIOLOGY & THERAPY
卷 3, 期 3, 页码 305-313出版社
TAYLOR & FRANCIS INC
DOI: 10.4161/cbt.3.3.697
关键词
Wee1; Chk1; Myt1 siRNA; G(2) checkpoint; apoptosis; p53; DNA damage
类别
Mammalian cells undergo cell cycle arrest in response to DNA damage due to the existence of multiple checkpoint response mechanisms. One such checkpoint pathway operating at the G(1) phase is frequently lost in cancer cells due to mutation of the p53 tumor suppressor gene. However, cancer cells often arrest at the G(2) phase upon DNA damage, due to activation of another checkpoint pathway that prevents the activation of Cdc2 kinase. The kinases, Chk1, Wee1, and Myt1 are key regulators of this G(2) checkpoint, which act directly or indirectly to inhibit Cdc2 activity. Here we show that RNA interference (RNAi)-mediated downregulation of Wee1 kinase abrogated an Adriamycin(R)-induced G(2) checkpoint in human cervical carcinoma Hela cells that are defective in G, checkpoint response. Wee1 downregulation sensitized HeLa cells to Adriamycin(R)-induced apoptosis. Downregulation of Chk1 kinase in Hela cells also caused a significant amount of cell death independent of DNA damage. In contrast, Myt1 downregulation abrogated Adriamycin(R)-induced G(2) arrest but did not cause substantial apoptosis. Reduction in Wee1, Chk1, or Myt1 levels did not sensitize normal human mammary epithelial cells (HMEC) cells to Adriamycin(R)-induced apoptosis unlike the situation in Hela cells. Our study reveals distinct roles for Chk1, Wee1, and Myt1 in G(2) checkpoint regulation. The data reported here support the attractiveness of Wee1 and Chk1 as molecular targets for abrogating the G2 DNA damage checkpoint arrest, a situation that may selectively sensitize p53-deficient tumor cells to radiation or chemotherapy treatment.
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