Literature DB >> 27090900

Prognostic Value of YKL-40 in Patients with Glioblastoma: a Systematic Review and Meta-analysis.

Gang Qin1, Xianfeng Li2, Zilong Chen3, Guangcha Liao1, Yu Su3, Yaode Chen3, Wei Zhang4.   

Abstract

YKL-40 is the most highly expressed gene in glioblastoma compared with normal brain tissues. Previous studies assessing the association between YKL-40 and survival in glioblastoma patients reported varying magnitude of estimates. The objective of this meta-analysis was to determine the prognostic value of YKL-40 in glioblastoma patients. PubMed and Embase databases were searched for studies relating to YKL-40 and prognosis of glioblastoma patients. Studies reporting estimates for overall survival by YKL-40 expression in glioblastoma patients were considered eligible. A meta-analysis of included studies was performed using fixed- or random-effect model to calculate the pooled hazard ratio (HR) and 95 % confidence interval (95%CI). Eight studies were ultimately considered eligible and included into the meta-analysis. Those eight studies included 1241 glioblastoma patients. Meta-analysis of those studies showed that high YKL-40 expression was associated with worse overall survival in glioblastoma patients (HR = 1.46, 95%CI 1.33-1.61, P < 0.001). Meta-analysis of studies with adjusted estimates and high quality showed that high YKL-40 expression was independently associated with worse overall survival in glioblastoma patients (HR = 1.50, 95%CI 1.35-1.66, P < 0.001). Both subgroup analysis and sensitivity analysis validated the obvious association between high YKL-40 expression and worse overall survival in glioblastoma patients. High YKL-40 expression is independently and markedly associated with worse overall survival in glioblastoma patients. YKL-40 is a good predictive biomarker of prognosis in glioblastoma patients.

Entities:  

Keywords:  Glioblastoma; Prognostic marker; YKL-40

Mesh:

Substances:

Year:  2016        PMID: 27090900     DOI: 10.1007/s12035-016-9878-2

Source DB:  PubMed          Journal:  Mol Neurobiol        ISSN: 0893-7648            Impact factor:   5.590


  36 in total

1.  Serum YKL-40 is a marker of prognosis and disease status in high-grade gliomas.

Authors:  Fabio M Iwamoto; Andreas F Hottinger; Sasan Karimi; Elyn Riedel; Jocelynn Dantis; Maryam Jahdi; Katherine S Panageas; Andrew B Lassman; Lauren E Abrey; Martin Fleisher; Lisa M DeAngelis; Eric C Holland; Adília Hormigo
Journal:  Neuro Oncol       Date:  2011-08-10       Impact factor: 12.300

2.  CHI3L1 (YKL-40) is expressed in human gliomas and regulates the invasion, growth and survival of glioma cells.

Authors:  Bo Mi Ku; Yeon Kyung Lee; Jinhyun Ryu; Joo Yeon Jeong; Jungil Choi; Keyoung Mi Eun; Hye Young Shin; Dong Gyu Kim; Eun Mi Hwang; Jae Cheal Yoo; Jae-Yong Park; Gu Seob Roh; Hyun Joon Kim; Gyeong Jae Cho; Wan Sung Choi; Sun Ha Paek; Sang Soo Kang
Journal:  Int J Cancer       Date:  2011-03-15       Impact factor: 7.396

Review 3.  Molecular characterizations of glioblastoma, targeted therapy, and clinical results to date.

Authors:  Jayson I L Bastien; Katharine A McNeill; Howard A Fine
Journal:  Cancer       Date:  2014-09-23       Impact factor: 6.860

4.  YKL-40 and matrix metalloproteinase-9 as potential serum biomarkers for patients with high-grade gliomas.

Authors:  Adília Hormigo; Bin Gu; Sasan Karimi; Elyn Riedel; Katherine S Panageas; Mark A Edgar; Meena K Tanwar; Jasti S Rao; Martin Fleisher; Lisa M DeAngelis; Eric C Holland
Journal:  Clin Cancer Res       Date:  2006-10-01       Impact factor: 12.531

5.  In vivo CHI3L1 (YKL-40) expression in astrocytes in acute and chronic neurological diseases.

Authors:  Dafna Bonneh-Barkay; Guoji Wang; Adam Starkey; Ronald L Hamilton; Clayton A Wiley
Journal:  J Neuroinflammation       Date:  2010-06-11       Impact factor: 8.322

6.  Epidermal growth factor receptor variant III status defines clinically distinct subtypes of glioblastoma.

Authors:  Christopher E Pelloski; Karla V Ballman; Alfred F Furth; Li Zhang; E Lin; Erik P Sulman; Krishna Bhat; J Matthew McDonald; W K Alfred Yung; Howard Colman; Shiao Y Woo; Amy B Heimberger; Dima Suki; Michael D Prados; Susan M Chang; Fred G Barker; Jan C Buckner; C David James; Kenneth Aldape
Journal:  J Clin Oncol       Date:  2007-06-01       Impact factor: 44.544

Review 7.  Diverse pathological implications of YKL-40: answers may lie in 'outside-in' signaling.

Authors:  Mansi Prakash; Manish Bodas; Divya Prakash; Neelu Nawani; Madhukar Khetmalas; Abul Mandal; Cecilia Eriksson
Journal:  Cell Signal       Date:  2013-04-02       Impact factor: 4.315

8.  Protein and mRNA levels of YKL-40 in high-grade glioma.

Authors:  M H Kazakova; D N Staneva; I G Koev; D G Staikov; N Mateva; P T Timonov; G A Miloshev; V S Sarafian
Journal:  Folia Biol (Praha)       Date:  2014       Impact factor: 0.906

Review 9.  The future of glioblastoma therapy: synergism of standard of care and immunotherapy.

Authors:  Mira A Patel; Jennifer E Kim; Jacob Ruzevick; Gordon Li; Michael Lim
Journal:  Cancers (Basel)       Date:  2014-09-29       Impact factor: 6.639

Review 10.  The role of cytotoxic chemotherapy in the management of progressive glioblastoma : a systematic review and evidence-based clinical practice guideline.

Authors:  Jeffrey J Olson; Lakshmi Nayak; D Ryan Ormond; Patrick Y Wen; Steven N Kalkanis
Journal:  J Neurooncol       Date:  2014-04-17       Impact factor: 4.130

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  6 in total

Review 1.  Older studies can underestimate prognosis of glioblastoma biomarker in meta-analyses: a meta-epidemiological study for study-level effect in the current literature.

Authors:  Victor M Lu; Kevin Phan; Julia X M Yin; Kerrie L McDonald
Journal:  J Neurooncol       Date:  2018-05-16       Impact factor: 4.130

Review 2.  Molecular and Circulating Biomarkers in Patients with Glioblastoma.

Authors:  Nadia Senhaji; Asmae Squalli Houssaini; Salma Lamrabet; Sara Louati; Sanae Bennis
Journal:  Int J Mol Sci       Date:  2022-07-05       Impact factor: 6.208

3.  YKL-40 in the brain and cerebrospinal fluid of neurodegenerative dementias.

Authors:  Franc Llorens; Katrin Thüne; Waqas Tahir; Eirini Kanata; Daniela Diaz-Lucena; Konstantinos Xanthopoulos; Eleni Kovatsi; Catharina Pleschka; Paula Garcia-Esparcia; Matthias Schmitz; Duru Ozbay; Susana Correia; Ângela Correia; Ira Milosevic; Olivier Andréoletti; Natalia Fernández-Borges; Ina M Vorberg; Markus Glatzel; Theodoros Sklaviadis; Juan Maria Torres; Susanne Krasemann; Raquel Sánchez-Valle; Isidro Ferrer; Inga Zerr
Journal:  Mol Neurodegener       Date:  2017-11-10       Impact factor: 14.195

4.  Elevated YKL-40 expression is associated with a poor prognosis in breast cancer patients.

Authors:  Guoxing Wan; Longchao Xiang; Xue Sun; Xuanbin Wang; Hongliang Li; Wei Ge; Fengjun Cao
Journal:  Oncotarget       Date:  2017-01-17

5.  Prognostic value of YKL-40 in solid tumors: a meta-analysis of 41 cohort studies.

Authors:  Bingxian Bian; Li Li; Junyao Yang; Yi Liu; Guohua Xie; Yingxia Zheng; Liang Zeng; Junxiang Zeng; Lisong Shen
Journal:  Cancer Cell Int       Date:  2019-10-10       Impact factor: 5.722

6.  Perspective: targeting VEGF-A and YKL-40 in glioblastoma - matter matters.

Authors:  Camilla Bjørnbak Holst; Henriette Pedersen; Elisabeth Anne Adanma Obara; Kristoffer Vitting-Seerup; Kamilla Ellermann Jensen; Jane Skjøth-Rasmussen; Eva Løbner Lund; Hans Skovgaard Poulsen; Julia Sidenius Johansen; Petra Hamerlik
Journal:  Cell Cycle       Date:  2021-03-28       Impact factor: 4.534

  6 in total

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