Lgr5 expression is a valuable prognostic factor for colorectal cancer: evidence from a meta-analysis

被引:18
作者
Jiang, Yangyan [1 ]
Li, Wenlu [2 ]
He, Xin [3 ]
Zhang, Hongbo [4 ]
Jiang, Fangzhen [5 ]
Chen, Zhigang [6 ]
机构
[1] Zhejiang Univ, Sch Med, Dept UItrason Diag, Affiliated Hosp 2, Hangzhou 310003, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Pharm, Dept Pharmacol, Hangzhou 310003, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Dept Hematol, Affiliated Hosp 2, Hangzhou 310003, Zhejiang, Peoples R China
[4] Third Peoples Hosp, Dept Neurol, Huzhou, Peoples R China
[5] Zhejiang Univ, Sch Med, Dept Plast Surg, Affiliated Hosp 2, Hangzhou 310003, Zhejiang, Peoples R China
[6] Zhejiang Univ, Sch Med, Dept Oncol, Affiliated Hosp 2, Hangzhou 310003, Zhejiang, Peoples R China
关键词
Lgr5; Prognostic value; Clinical-pathological differences; Colorectal cancer; Meta-analysis; PROTEIN-COUPLED RECEPTOR; STEM-CELL MARKER; COLON-CANCER; OVER-EXPRESSION; OVEREXPRESSION; GPR49; STATISTICS; CARCINOMA; SURVIVAL; PATIENT;
D O I
10.1186/s12885-015-1985-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Lgr5 has recently been identified as a reliable biomarker of cancer stem cells (CSCs) in colorectal cancer (CRC); however, its prognostic value is still controversial. Methods: We searched PubMed, Web of Science, and Wanfang databases with identical strategies to retrieve articles. We evaluated the impact of Lgr5 expression on survival of CRC patients through meta-analysis. Results: A total of 12 studies comprising 2600 patients revealed that Lgr5 overexpression was negatively associated with overall survival (OS) (HR = 1.73, 95 % CI: 1.28-2.33; P = 0.00) and disease free survival (DFS) (HR = 2.89, 95 % CI: 1.89-4.44; P = 0.000) in CRC patients. Subgroup analysis suggested that Lgr5 overexpression was significantly associated with worse OS in subgroups with IHC as the method of Lgr5 assessment (HR = 2.01, 95 % CI: 1.39-2.89; P = 0.001), patients from Asia (HR = 1.81, 95 % CI: 1.27-2.58; P = 0.000), and NOS scores greater than 6 (HR = 2.12, 95 % CI: 1.41-3.19; P = 0.000). Furthermore, sensitivity analysis showed that the estimated HR ranged from 1.6 to 1.86 upon excluding one study sequentially from each analysis. In addition, Lgr5 overexpression was significantly associated with deep invasion of CRC (OR = 0.39, 95 % CI: 0.17-0.87; P = 0.002), lymphnode metastasis (OR = 0.45, 95 % CI: 0.26-0.76; P = 0.003), distant metastasis (OR = 0.37, 95 % CI: 0.22-0.62; P = 0.000), and AJCC stage (OR = 0.35, 95 % CI: 0.15-0.78; P = 0.01). However, Lgr5 overexpression was not correlated with tumor grade (OR = 0.75 95 % CI: 0.37-1.54; P = 0.433). Conclusions: This study shows that Lgr5 can be a valuable and reliable prognostic factor of colorectal cancer progression.
引用
收藏
页数:10
相关论文
共 35 条
  • [1] Cancer stem cells in solid tumors
    Ailles, Laurie E.
    Weissman, Irving L.
    [J]. CURRENT OPINION IN BIOTECHNOLOGY, 2007, 18 (05) : 460 - 466
  • [2] [Anonymous], MODERN DIGESTION INT
  • [3] [Anonymous], LIN CHUANG JIAN YAN
  • [4] [Anonymous], NATURE
  • [5] [Anonymous], INT J COLORECTAL DIS
  • [6] Adjuvant therapy for colon cancer
    Aranha O.
    Benson III A.B.
    [J]. Current Gastroenterology Reports, 2007, 9 (5) : 415 - 421
  • [7] Immunostaining of Lgr5, an Intestinal Stem Cell Marker, in Normal and Premalignant Human Gastrointestinal Tissue
    Becker, Laren
    Huang, Qin
    Mashimo, Hiroshi
    [J]. THESCIENTIFICWORLDJOURNAL, 2008, 8 : 1168 - 1176
  • [8] Increased expression of CD133 and reduced dystroglycan expression are strong predictors of poor outcome in colon cancer patients
    Coco, Claudio
    Zannoni, Gian Franco
    Caredda, Emanuele
    Sioletic, Stefano
    Boninsegna, Alma
    Migaldi, Mario
    Rizzo, Gianluca
    Bonetti, Luca Reggiani
    Genovese, Giannicola
    Stigliano, Egidio
    Cittadini, Achille
    Sgambato, Alessandro
    [J]. JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2012, 31
  • [9] Apoptosis signaling in cancer stem cells
    Fulda, Simone
    Pervaiz, Shazib
    [J]. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2010, 42 (01) : 31 - 38
  • [10] Gao FJ, 2014, INT J CLIN EXP PATHO, V7, P1572