Identification of mRNAs modulated by knockdown of CD24

ABSTRACT: We endeavored to identify factors and pathways regulated by CD24 and to obtain leads regarding the mechanism by which CD24 inhibited the invasiveness and metastasis of pancreatic cancer cells by performing cDNA microarray analysis on S2-013 CD24 RNAi clones and control clones. The group of genes showing increased expression was mainly comprised of genes for molecules with functions related to RNA metabolism, transcription factors, proteases, and molecules involved in embryonic development and cell growth. The set of genes downregulated by knockdown of CD24 included the target mRNAs of a phosphorylation-dependent endoribonuclease G3BP that interacted with CD24. The target mRNAs of G3BP were identified in GSE17056. These results suggested that CD24 inhibited the RNase activity of G3BP, and t

ORGANISM(S): Homo sapiens

SUBMITTER: Keisuke Taniuchi 

PROVIDER: E-GEOD-17055 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress