PIM Kinase as an Executional Target in Cancer
Xinning Zhang(Henan Cancer Hospital), Mengqiu Song(Zhengzhou University), Joydeb Kumar Kundu(University of Alberta), Mee‐Hyun Lee(Zhengzhou University), Zhenzhen Liu(Zhengzhou University)
Cited by 130Open Access
Abstract
PIM (proviral integration site for moloney murine leukemia virus) kinase plays a key role as an oncogene in various cancers including myeloma, leukemia, prostate and breast cancers. The aberrant expression and/or activation of PIM kinases in various cancers follow an isoform-specific pattern. While PIM1 is predominantly expressed in hematological and solid tumors, PIM2 and PIM3 are largely expressed in leukemia and solid tumors, respectively. All of PIM kinases cause transcriptional activation of genes involved in cell survival and cell cycle progression in cancer. A variety of pro-tumorigenic signaling molecules, such as MYC, p21
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