microRNA expression profile in undifferentiated gastric cancer

被引:281
作者
Katada, Takeyasu [1 ]
Ishiguro, Hideyuki [1 ]
Kuwabara, Yoshiyuki [1 ]
Kimura, Masahiro [1 ]
Mitui, Akira [1 ]
Mori, Yoichiro [1 ]
Ogawa, Ryo [1 ]
Harata, Koshiro [1 ]
Fujii, Yoshitaka [1 ]
机构
[1] Nagoya City Univ, Grad Sch Med Sci Oncol Immunol & Surg, Mizuho Ku, Nagoya, Aichi 4678601, Japan
关键词
microRNA; undifferentiated gastric cancer; profile; quantitative reverse transcriptase-polymerase chain reaction; CELL-CYCLE ARREST; GENE-EXPRESSION; CARCINOMA; APOPTOSIS; GROWTH; INVOLVEMENT; INHIBITION; SUPPRESSOR; INDUCTION; MIRNAS;
D O I
10.3892/ijo_00000179
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prognosis of patients with undifferentiated gastric cancer is generally poor. The expression of various microRNAs (miRNAs) has not been comprehensively investigated in undifferentiated gastric cancer. Total RNA was extracted from the specimens of 42 undifferentiated gastric cancer tissues and paired normal gastric tissue. Quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) was performed for a set of 72 miRNAs. The expression of each miRNA relative to the internal control RNA was determined using the 2(Delta Ct) method, The expression levels of 3 miRNAs (mir-34b, mir-34c and mir-128a) were significantly upregulated and those of 3 miRNAs (mir-128b, mir-129 and mir-149) were downregulated in undifferentiated gastric cancer tissue when compared with those of the paired normal tissues. The probability of survival was significantly lower in patients with high expression levels of mir-20b or 150. There was a correlation between mir-27a and lymph node metastasis. Our investigation provides a list of candidate miRNAs that may be associated with the prognosis in undifferentiated gastric cancer patients. Further study is warranted to identify the target genes of these miRNAs and their function.
引用
收藏
页码:537 / 542
页数:6
相关论文
共 37 条
[1]  
Adachi Y, 2000, CANCER-AM CANCER SOC, V89, P1418
[2]   let-7 microRNA functions as a potential growth suppressor in human colon cancer cells [J].
Akao, Yukihiro ;
Nakagawa, Yoshihito ;
Naoe, Tomoki .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2006, 29 (05) :903-906
[3]   MicroRNA functions in animal development and human disease [J].
Alvarez-Garcia, I ;
Miska, EA .
DEVELOPMENT, 2005, 132 (21) :4653-4662
[4]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[5]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[6]   The role of the STAT5 proteins in the proliferation and apoptosis of the CML and AML cells [J].
Baskiewicz-Masiuk, M ;
Machalinski, B .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2004, 72 (06) :420-429
[7]   Effect of ret/PTC 1 rearrangement on transcription and post-transcriptional regulation in a papillary thyroid carcinoma model [J].
Cahill, Susanne ;
Smyth, Paul ;
Finn, Stephen P. ;
Denning, Karen ;
Flavin, Richard ;
O'Regan, Esther M. ;
Li, Jinghuan ;
Potratz, Astrid ;
Guenther, Simone M. ;
Henfrey, Richard ;
O'Leary, John J. ;
Sheils, Orla .
MOLECULAR CANCER, 2006, 5 (1)
[8]   Antisense inhibition of human miRNAs and indications for an involvement of miRNA in cell growth and apoptosis [J].
Cheng, AM ;
Byrom, MW ;
Shelton, J ;
Ford, LP .
NUCLEIC ACIDS RESEARCH, 2005, 33 (04) :1290-1297
[9]   IGF-independent effects of IGFBP-2 on the human breast cancer cell line Hs578T [J].
Frommer, Klaus W. ;
Reichenmiller, Katharina ;
Schutt, Burkhardt S. ;
Hoeflich, Andreas ;
Ranke, Michael B. ;
Dodt, Gabriele ;
Elmlinger, Martin W. .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2006, 37 (01) :13-23
[10]  
Fukuda Y, 2000, GENE CHROMOSOME CANC, V29, P315, DOI 10.1002/1098-2264(2000)9999:9999<::AID-GCC1047>3.0.CO