MicroRNAs as a potential prognostic factor in gastric cancer

被引:183
作者
Brenner, Baruch [1 ,2 ]
Hoshen, Moshe B. [3 ,4 ]
Purim, Ofer [1 ,2 ]
Ben David, Miriam [3 ]
Ashkenazi, Karin [3 ]
Marshak, Gideon [2 ,6 ]
Kundel, Yulia [2 ]
Brenner, Ronen [2 ]
Morgenstern, Sara [2 ]
Halpern, Marisa [2 ,6 ]
Rosenfeld, Nitzan [5 ]
Chajut, Ayelet [3 ]
Niv, Yaron [2 ,7 ]
Kushnir, Michal [3 ]
机构
[1] Beilinson Med Ctr, Rabin Med Ctr, Davidoff Ctr, Inst Oncol, IL-49100 Petah Tiqwa, Israel
[2] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
[3] Rosetta Genom Ltd, IL-76706 Rehovot, Israel
[4] Clalit Res Inst, Clalit Med Serv, IL-69978 Tel Aviv, Israel
[5] Cambridge Res Inst, Canc Res UK, Cambridge CB2 ORE, England
[6] Golda Hasharon Hosp, Rabin Med Ctr, Inst Oncol, IL-49100 Petah Tiqwa, Israel
[7] Beilinson Med Ctr, Rabin Med Ctr, Dept Gastroenterol, IL-49100 Petah Tiqwa, Israel
关键词
MicroRNA; Prognosis; Recurrence; Gastric cancer; BREAST-CANCER; EXPRESSION; CELLS; SIGNATURES; ADENOCARCINOMA; SURVIVAL; SURGERY; MARKER; IMPACT;
D O I
10.3748/wjg.v17.i35.3976
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
AIM: To compare the microRNA (miR) profiles in the primary tumor of patients with recurrent and non-recurrent gastric cancer. METHODS: The study group included 45 patients who underwent curative gastrectomies from 1995 to 2005 without adjuvant or neoadjuvant therapy and for whom adequate tumor content was available. Total RNA was extracted from formalin-fixed paraffin-embedded tumor samples, preserving the small RNA fraction. Initial profiling using miR microarrays was performed to identify potential biomarkers of recurrence after resection. The expression of the differential miRs was later verified by quantitative real-time polymerase chain reaction (qRT-PCR). Findings were compared between patients who had a recurrence within 36 mo of surgery (bad-prognosis group, n = 14, 31%) and those who did not (good-prognosis group, n = 31, 69%). RESULTS: Three miRs, miR-451, miR-199a-3p and miR-195 were found to be differentially expressed in tumors from patients with good prognosis vs patients with bad prognosis (P < 0.0002, 0.0027 and 0.0046 respectively). High expression of each miR was associated with poorer prognosis for both recurrence and survival. Using miR-451, the positive predictive value for non-recurrence was 100% (13/13). The expression of the differential miRs was verified by qRT-PCR, showing high correlation to the microarray data and similar separation into prognosis groups. CONCLUSION: This study identified three miRs, miR-451, miR-199a-3p and miR-195 to be predictive of recurrence of gastric cancer. Of these, miR-451 had the strongest prognostic impact.
引用
收藏
页码:3976 / 3985
页数:10
相关论文
共 34 条
[1]
Role of miRNA in carcinogenesis and biomarker selection: a methodological view [J].
Ahmed, Farid E. .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2007, 7 (05) :569-603
[2]
Prognostic value of age and sex in early gastric cancer [J].
Bando, E ;
Kojima, N ;
Kawamura, T ;
Takahashi, S ;
Fukushima, N ;
Yonemura, Y .
BRITISH JOURNAL OF SURGERY, 2004, 91 (09) :1197-1201
[3]
microRNA-451 Regulates Macrophage Migration Inhibitory Factor Production and Proliferation of Gastrointestinal Cancer Cells [J].
Bandres, Eva ;
Bitarte, Nerea ;
Arias, Fernando ;
Agorreta, Jackeline ;
Fortes, Puri ;
Agirre, Xabi ;
Zarate, Ruth ;
Diaz-Gonzalez, Juan A. ;
Ramirez, Natalia ;
Sola, Jesus J. ;
Jimenez, Paula ;
Rodriguez, Javier ;
Garcia-Foncillas, Jesus .
CLINICAL CANCER RESEARCH, 2009, 15 (07) :2281-2290
[4]
Identification of hundreds of conserved and nonconserved human microRNAs [J].
Bentwich, I ;
Avniel, A ;
Karov, Y ;
Aharonov, R ;
Gilad, S ;
Barad, O ;
Barzilai, A ;
Einat, P ;
Einav, U ;
Meiri, E ;
Sharon, E ;
Spector, Y ;
Bentwich, Z .
NATURE GENETICS, 2005, 37 (07) :766-770
[5]
Polymorphisms in predicted microRNA-binding sites in integrin genes and breast cancer:: ITGB4 as prognostic marker [J].
Brendle, Annika ;
Lei, Haixin ;
Brandt, Andreas ;
Johansson, Robert ;
Enquist, Kerstin ;
Henriksson, Roger ;
Hemminki, Kari ;
Lenner, Per ;
Foersti, Asta .
CARCINOGENESIS, 2008, 29 (07) :1394-1399
[6]
MicroRNA signatures in human cancers [J].
Calin, George A. ;
Croce, Carlo M. .
NATURE REVIEWS CANCER, 2006, 6 (11) :857-866
[7]
Perioperative chemotherapy versus surgery alone for resectable gastroesophageal cancer [J].
Cunningham, David ;
Allum, William H. ;
Stenning, Sally P. ;
Thompson, Jeremy N. ;
Van de Velde, Cornelis J. H. ;
Nicolson, Marianne ;
Scarffe, J. Howard ;
Lofts, Fiona J. ;
Falk, Stephen J. ;
Iveson, Timothy J. ;
Smith, David B. ;
Langley, Ruth E. ;
Verma, Monica ;
Weeden, Simon ;
Chua, Yu Jo .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (01) :11-20
[8]
EDGE SB, 2010, AJCC CANC STAGING MA, P147
[9]
The widespread impact of mammalian microRNAs on mRNA repression and evolution [J].
Farh, KKH ;
Grimson, A ;
Jan, C ;
Lewis, BP ;
Johnston, WK ;
Lim, LP ;
Burge, CB ;
Bartel, DP .
SCIENCE, 2005, 310 (5755) :1817-1821
[10]
Serum MicroRNAs Are Promising Novel Biomarkers [J].
Gilad, Shlomit ;
Meiri, Eti ;
Yogev, Yariv ;
Benjamin, Sima ;
Lebanony, Danit ;
Yerushalmi, Noga ;
Benjamin, Hila ;
Kushnir, Michal ;
Cholakh, Hila ;
Melamed, Nir ;
Bentwich, Zvi ;
Hod, Moshe ;
Goren, Yaron ;
Chajut, Ayelet .
PLOS ONE, 2008, 3 (09)