Evidence map›Paper›PMID 32306128›Full record

ArticleJournal of cancer research and clinical oncology2020

High MICB expression as a biomarker for good prognosis of colorectal cancer.

Qingyang Feng, Shanchao Yu, Yihao Mao, Meiling Ji, Ye Wei, Guodong He, Wenju Chang, Dexiang Zhu, Li Ren, Jianmin Xu

Open access · hybridAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  5. Review
  6. Review
  7. Article
  8. Associations between MICA and MICB Genetic Variants, Protein Levels, and Colorectal Cancer: Atherosclerosis Risk in Communities (ARIC).Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2023
    Article
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  11. Review
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  13. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Qingyang FengDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Shanchao YuDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Yihao MaoDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Meiling JiDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Ye WeiDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Guodong HeDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Wenju ChangDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Dexiang ZhuDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Li RenDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China. renli1969@foxmail.com.
Jianmin XuDepartment of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China. xujmin@aliyun.com.ORCID http://orcid.org/0000-0001-5441-8240
Sun Yat-sen University · CN

Funding

Excellent Youth Talent Development Program of Zhongshan Hospital, Fudan University 2019ZSYXQN03National Natural Science Foundation of China 81602040
6 · The paper itself

Abstract

introductionMajor histocompatibility complex (MHC) plays an important role in colorectal cancer (CRC) immunity. However, the function of MHC class I chain-related B (MICB) molecule is not very clear. In this study, we explored the prognostic effect of MICB in colorectal cancer. MATERIAL AND

methodsFrom 2008-05 to 2012-11, consecutive CRC patients of Zhongshan Hospital, Fudan University were retrospectively enrolled as primary cohort. The inclusion criteria were as follows: receiving primary radical resection, pathologically confirmed colorectal adenocarcinoma, no treatment before surgery, clinicopathological data available. Another cohort of CRC patients were collected from a public dataset GSE39582 of GEO database from 1987 to 2007 in the same criteria for validation. MICB was detected using immunochemistry and evaluated as prognostic biomarker. The cut-off value of MICB expression was calculated using X-tile software.

resultsFinally, 863 patients were enrolled in the primary cohort, and 556 patients were enrolled in the validation cohort. MICB expression was significantly associated with tumor size and primary histological type in primary cohort, and with primary tumor location and distant metastases in validation cohort. The survival analysis showed that patients with high MICB expression had significantly better overall survival in both primary (P = 0.002) and validation (P = 0.001) cohorts. The multivariate analysis also confirmed that high MICB expression was a significantly independent protective factor for overall survival in both primary (hazard ratio HR = 0.741, 95% CI 0.594-0.924) and validation (HR = 0.699, 95% CI 0.508-0.961) cohorts.

conclusionFor stage I-IV CRC patients, MICB was confirmed a novel independent prognostic factor. It could help better stratification of CRC prognosis.

Indexed as

Biomarkers, TumorColorectal NeoplasmsFemaleHistocompatibility Antigens Class IHumansMaleMiddle AgedPrognosisRetrospective StudiesSurvival AnalysisBiomarkers, TumorHistocompatibility Antigens Class IMICB antigenColorectal cancerMICBPrognosis

Identifiers

PMID32306128
PMCPMC7230058
OpenAlexW3016824004

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.