Increased Expression of DNAJC12 is Associated with Aggressive Phenotype of Gastric Cancer.

Abstract:

BACKGROUND:Identification of gastric cancer-related molecules is necessary to elucidate the pathological mechanisms of this heterogeneous disease. The purpose of this study was to identify novel genes associated with aggressive phenotypes of gastric cancer. METHODS:Global expression profiling was conducted using tissues from four patients with metastatic gastric cancer to identify genes overexpressed in gastric cancer. Fifteen gastric cell lines and 262 pairs of surgically resected gastric tissues were subjected to mRNA expression analysis. The contribution of the candidate gene on gastric cancer cell proliferation, invasion, adhesion, and migration were evaluated using small interfering RNA. RESULTS:DnaJ heat shock protein family (Hsp40) member C12 (DNAJC12) was identified as a candidate gene by transcriptome analysis. In clinical samples, DNAJC12 mRNA levels were higher in gastric cancer tissues compared with normal adjacent tissues. Patients with high DNAJC12 expression showed significantly shorter overall survival in our cohort and in the extra-validation cohort analyzed by a published microarray dataset. High DNAJC12 expression in gastric cancer tissues was significantly associated with lymphatic involvement, infiltrative growth type, lymph node metastasis, and advanced stage and was identified as an independent prognostic factor for overall survival in multivariable analysis. Increased expression of DNAJC12 was found in 12 of 14 examined gastric cancer cell lines. Knockdown of DNAJC12 expression significantly decreased the proliferation and invasion abilities of gastric cancer cells. CONCLUSIONS:Our findings support DNAJC12 as a candidate gene associated with aggressive phenotypes of gastric cancer.

journal_name

Ann Surg Oncol

authors

Uno Y,Kanda M,Miwa T,Umeda S,Tanaka H,Tanaka C,Kobayashi D,Suenaga M,Hattori N,Hayashi M,Yamada S,Nakayama G,Fujiwara M,Kodera Y

doi

10.1245/s10434-018-07149-y

subject

Has Abstract

pub_date

2019-03-01 00:00:00

pages

836-844

issue

3

eissn

1068-9265

issn

1534-4681

pii

10.1245/s10434-018-07149-y

journal_volume

26

pub_type

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