Clinical Significance of KIAA1199 as a Novel Target for Gastric Cancer Drug Therapy

被引:17
|
作者
Oneyama, Masataka [1 ,2 ]
Sakamoto, Naoya [3 ]
Oue, Naohide [3 ]
Kimura, Yayoi [4 ]
Hiroshima, Yukihiko [5 ]
Hashimoto, Itaru [2 ]
Hara, Kentaro [2 ]
Maezawa, Yukio [6 ]
Kano, Kazuki [1 ]
Aoyama, Toru [2 ]
Fujikawa, Hirohito [1 ]
Yamada, Takanobu [1 ]
Tamagawa, Hiroshi [2 ]
Yamamoto, Naoto [1 ]
Ogata, Takashi [1 ]
Cho, Haruhiko [6 ]
Ito, Hiroyuki [7 ]
Yukawa, Norio [2 ]
Shiozawa, Manabu [1 ]
Yoshikawa, Takaki [8 ]
Morinaga, Soichiro [1 ]
Rino, Yasushi [2 ]
Masuda, Munetaka [2 ]
Miyagi, Yohei [5 ]
Yasui, Wataru [3 ]
Oshima, Takashi [1 ]
机构
[1] Kanagawa Canc Ctr, Dept Gastrointestinal Surg, Yokohama, Kanagawa 2418515, Japan
[2] Yokohama City Univ, Dept Surg, Yokohama, Kanagawa, Japan
[3] Hiroshima Univ, Dept Mol Pathol, Inst Biomed & Hlth Sci, Hiroshima, Japan
[4] Yokohama City Univ, Adv Med Res Ctr, Yokohama, Kanagawa, Japan
[5] Kanagawa Canc Ctr, Res Inst, Yokohama, Kanagawa, Japan
[6] Komagome Hosp, Dept Surg, Tokyo Metropolitan Canc & Infect Dis Ctr, Tokyo, Japan
[7] Kanagawa Canc Ctr, Dept Resp Surg, Yokohama, Kanagawa, Japan
[8] Natl Canc Ctr, Dept Gastr Surg, Tokyo, Japan
关键词
KIAA1199; gastric cancer; prognostic factor; S-1; ADJUVANT CHEMOTHERAPY; OPEN-LABEL; GENE; CAPECITABINE; OXALIPLATIN; PROTEIN; CELLS; S-1;
D O I
10.21873/anticanres.13872
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: The KIAA1199 gene has been associated with cancer- cell proliferation, but its functions remain poorly studied. Here, we examined the clinical significance of the KIAA1199 mRNA levels in locally advanced gastric cancer (GC). Materials and Methods/Results: Using samples from 254 patients with stage II/III GC, we found significantly higher KIAA1199 levels in cancerous tissues compared to adjacent normal mucosa (ANM). There was no significant relationship between KIAA1199 expression and clinical features. Although overall survival rates (OSR) of patients, who underwent surgery did not correlate with KIAA1199 expression, patients who underwent adjuvant chemotherapy with S-1 and had high KIAA1199 levels displayed significantly lower OSR. KIAA1199 knock down (KIAA1199-KD) suppressed proliferation, invasiveness, and sensitivity of GC cells to 5-fluorouracil (5-FU). Conclusion: KIAA1199 expression appears to be a promising prognostic marker in patients with locally advanced GC, who underwent postoperative adjuvant chemotherapy with S-1. KIAA1199 may represent a novel target for GC pharmacotherapy.
引用
收藏
页码:6567 / 6573
页数:7
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