Prognostic and clinicopathological significance of MLKL expression in cancer patients: a meta-analysis

被引:17
作者
Hu, Binwu [1 ]
Shi, Deyao [1 ]
Lv, Xiao [1 ]
Chen, Songfeng [2 ]
Huang, Qin [3 ]
Xie, Mao [1 ]
Shao, Zengwu [1 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Orthopaed, Wuhan 430022, Hubei, Peoples R China
[2] Zhengzhou Univ, Dept Orthopaed Surg, Affiliated Hosp 1, Zhengzhou, Henan, Peoples R China
[3] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Med Rehabil, Wuhan 430022, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
MLKL; Necroptosis; Cancer; Prognosis; Meta-analysis; MIXED LINEAGE KINASE; DOMAIN-LIKE PROTEIN; NECROPTOSIS; STATISTICS; SURVIVAL; NECROSIS; METHYLATION; APOPTOSIS; BIOMARKER; IMMUNE;
D O I
10.1186/s12885-018-4655-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: MLKL is the most important executor of necroptosis pathway. Recent studies have demonstrated that MLKL could serve as a potential prognostic biomarker for cancer patients. However, most studies reported so far are limited in discrete outcome and sample size. Methods: We systematically searched PubMed, Embase, Web of Science and CNKI to obtain all relevant articles about the prognostic value of abnormally expressed MLKL in patients with any type of tumor. Odds ratios or hazards ratios (HRs) with corresponding 95% confidence intervals (CIs) were pooled to estimate the association between MLKL expression and clinicopathological characteristics or survival of cancer patients. Results: A total of 6 eligible studies with 613 cancer patients were enrolled in our meta-analysis. Our results demonstrated that decreased expression level of MLKL was significantly associated with poor overall survival (OS) (pooled HR 0.26, 95%CI 0.17-040, high/low) and event-free survival (EFS) (pooled HR 0.45, 95%CI 0.23-0.87, high/ low) in cancer patients. Furthermoie, subgroup analysis divided by type of cancer, sample size, follow-up time and Newcastle-Ottawa Scale (NOS) score showed consistent prognostic value. In addition, our analysis revealed that decreased expression level of MLKL was significantly associated with advanced tumor stage, more lymph node metastasis and older age. Conclusions: In conclusion, our meta-analysis suggested that decreased MLKL expression might be a convinced unfavorable prognostic factor that could help the clinical decision-making process.
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页数:10
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共 32 条
  • [1] Altman DG, 2012, BMC MED, V10, DOI [10.1186/1741-7015-10-51, 10.1371/journal.pmed.1001216]
  • [2] Plasma membrane translocation of trimerized MLKL protein is required for TNF-induced necroptosis
    Cai, Zhenyu
    Jitkaew, Siriporn
    Zhao, Jie
    Chiang, Hsueh-Cheng
    Choksi, Swati
    Liu, Jie
    Ward, Yvona
    Wu, Ling-gang
    Liu, Zheng-Gang
    [J]. NATURE CELL BIOLOGY, 2014, 16 (01) : 55 - +
  • [3] Genetic variation in 1253 immune and inflammation genes and risk of non-Hodgkin lymphoma
    Cerhan, James R.
    Ansell, Stephen M.
    Fredericksen, Zachary S.
    Kay, Neil E.
    Liebow, Mark
    Call, Timothy G.
    Dogan, Ahmet
    Cunningham, Julie M.
    Wang, Alice H.
    Liu-Mares, Wen
    Macon, William R.
    Jelinek, Diane
    Witzig, Thomas E.
    Habermann, Thomas M.
    Slager, Susan L.
    [J]. BLOOD, 2007, 110 (13) : 4455 - 4463
  • [4] Necroptosis: an alternative cell death program defending against cancer
    Chen, Dongshi
    Yu, Jian
    Zhang, Lin
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2016, 1865 (02): : 228 - 236
  • [5] Cancer Statistics in China, 2015
    Chen, Wanqing
    Zheng, Rongshou
    Baade, Peter D.
    Zhang, Siwei
    Zeng, Hongmei
    Bray, Freddie
    Jemal, Ahmedin
    Yu, Xue Qin
    He, Jie
    [J]. CA-A CANCER JOURNAL FOR CLINICIANS, 2016, 66 (02) : 115 - 132
  • [6] Pronecrotic mixed lineage kinase domain-like protein expression is a prognostic biomarker in patients with early-stage resected pancreatic adenocarcinoma
    Colbert, Lauren E.
    Fisher, Sarah B.
    Hardy, Claire W.
    Hall, William A.
    Saka, Burcu
    Shelton, Joseph W.
    Petrova, Aleksandra V.
    Warren, Matthew D.
    Pantazides, Brooke G.
    Gandhi, Khanjan
    Kowalski, Jeanne
    Kooby, David A.
    El-Rayes, Bassel F.
    Staley, Charles A., III
    Adsay, N. Volkan
    Curran, Walter J., Jr.
    Landry, Jerome C.
    Maithel, Shishir K.
    Yu, David S.
    [J]. CANCER, 2013, 119 (17) : 3148 - 3155
  • [7] Long noncoding RNAs as auxiliary biomarkers for gastric cancer screening: A pooled analysis of individual studies
    Cui, Zhaolei
    Chen, Yan
    Xiao, Zhenzhou
    Hu, Minhua
    Lin, Yingying
    Chen, Yansong
    Zheng, Yuhong
    [J]. ONCOTARGET, 2016, 7 (18) : 25791 - 25800
  • [8] Microarray analysis of promoter methylation in lung cancers
    Fukasawa, M
    Kimura, M
    Morita, S
    Matsubara, K
    Yamanaka, S
    Endo, C
    Sakurada, A
    Sato, M
    Kondo, T
    Horii, A
    Sasaki, H
    Hatada, I
    [J]. JOURNAL OF HUMAN GENETICS, 2006, 51 (04) : 368 - 374
  • [9] The hallmarks of cancer
    Hanahan, D
    Weinberg, RA
    [J]. CELL, 2000, 100 (01) : 57 - 70
  • [10] He L, 2013, ONCOTARGETS THER, V6, P1539, DOI [10.2147/OTT.SS2805, 10.2147/OTT.S52805]