Annals of surgical oncology · 2013
Up-regulation of NEK2 by microRNA-128 methylation is associated with poor prognosis in colorectal cancer.
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Takahashi Yusuke, Iwaya Takeshi, Sawada Genta, Kurashige Junji, Matsumura Tae, Uchi Ryutaro, Ueo Hiroki, Takano Yuki, Eguchi Hidetoshi, Sudo Tomoya, Sugimachi Keishi, Yamamoto Hirofumi, Doki Yuichiro, Mori Masaki, Mimori Koshi
Аннотация
BACKGROUND: NIMA-related kinase 2 (NEK2), an enzyme involved in the development and progression of cancer, is abnormally expressed in a wide variety of human cancers, including colorectal cancer (CRC), and is known to have roles in cell division and mitotic regulation through centrosome splitting. We investigated the clinical significance of NEK2 in CRC. In particular, we examined miR-128 expression, which is thought to target NEK2.
METHODS: We measured NEK2 mRNA and miR-128 levels in clinical samples by quantitative reverse transcription real-time PCR and analyzed the associations between NEK2 levels, miR-128 levels, clinicopathological factors, and prognoses. Furthermore, we performed in vitro assays using a pre-miR-128 precursor and conducted miR-128 methylation analyses.
RESULTS: MiR-128 inhibited NEK2 expression and cancer cell proliferation via cell cycle arrest. Moreover, miR-128 was silenced by DNA methylation. Increased NEK2 expression was associated with serosal invasion, lymphatic invasion, and peritoneal dissemination. Patients with high NEK2 expression also had significantly poorer prognoses. Multivariate analysis indicated that high NEK2 expression was an independent prognostic factor for survival. Patients with high miR-128 expression had significantly lower NEK2 expression and lower recurrence rates than those with low miR-128 expression.
CONCLUSIONS: NEK2 may be an independent prognostic factor for CRC and was regulated by miR-128, a microRNA that was subjected to epigenetic regulation. Thus, this miR-128/NEK2 pathway may be a prospective therapeutic target for patients with CRC.
METHODS: We measured NEK2 mRNA and miR-128 levels in clinical samples by quantitative reverse transcription real-time PCR and analyzed the associations between NEK2 levels, miR-128 levels, clinicopathological factors, and prognoses. Furthermore, we performed in vitro assays using a pre-miR-128 precursor and conducted miR-128 methylation analyses.
RESULTS: MiR-128 inhibited NEK2 expression and cancer cell proliferation via cell cycle arrest. Moreover, miR-128 was silenced by DNA methylation. Increased NEK2 expression was associated with serosal invasion, lymphatic invasion, and peritoneal dissemination. Patients with high NEK2 expression also had significantly poorer prognoses. Multivariate analysis indicated that high NEK2 expression was an independent prognostic factor for survival. Patients with high miR-128 expression had significantly lower NEK2 expression and lower recurrence rates than those with low miR-128 expression.
CONCLUSIONS: NEK2 may be an independent prognostic factor for CRC and was regulated by miR-128, a microRNA that was subjected to epigenetic regulation. Thus, this miR-128/NEK2 pathway may be a prospective therapeutic target for patients with CRC.
Предметные рубрики MeSH
AgedApoptosisBiomarkers, TumorBlotting, WesternCell CycleCell ProliferationColorectal NeoplasmsDNA MethylationFemaleFollow-Up StudiesHumansLiver NeoplasmsLymphatic MetastasisMaleMicroRNAsNIMA-Related KinasesNeoplasm InvasivenessNeoplasm StagingPeritoneal NeoplasmsPrognosisProtein Serine-Threonine KinasesRNA, MessengerRNA, Small InterferingReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionSurvival RateTumor Cells, CulturedUp-Regulation