Evidence map›Paper›PMID 33163281›Full record

ArticleAmerican journal of cancer research2020

Prognostic value of leukocyte telomere length in renal cell carcinoma patients.

Meng Chen, Chia-Wen Tsai, Wen-Shin Chang, Junfeng Xu, Yifan Xu, Da-Tian Bau, Jian Gu

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Meng ChenDepartment of Clinical Laboratory, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College Beijing, China.
Chia-Wen TsaiDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center Houston, TX 77030, USA.
Wen-Shin ChangDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center Houston, TX 77030, USA.
Junfeng XuDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center Houston, TX 77030, USA.
Yifan XuDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center Houston, TX 77030, USA.
Da-Tian BauTerry Fox Cancer Research Laboratory, China Medical University Hospital Taichung, Taiwan.
Jian GuDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center Houston, TX 77030, USA.
Asia University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Telomeres play important roles in cancer initiation and progression. Leukocyte telomere length (LTL) can modulate cancer risk and outcome. We hypothesize that genetically predicted short LTL is associated with worse prognosis in renal cell carcinoma (RCC). A total of 1,086 histologically confirmed RCC patients were included in this study. A weighted genetic risk score (GRS) predictive of LTL was constructed using 10 confirmed LTL-associated single nucleotide polymorphisms (SNPs). The associations of individual SNPs and GRS with recurrence and survival were determined by multivariate Cox proportional hazards analysis. In individual SNP analysis, long LTL-associated allele of rs7675998 in NAF1 gene at chromosome 4 was significantly associated with a reduced risk of recurrence (HR=0.85, 95% CI, 0.73-0.99, P=0.043), while the long LTL-associated allele of rs10936599 in TERC at chromosome 3 conferred a reduced risk of death (HR=0.85, 95% CI, 0.73-1.00, P=0.047). More importantly, genetically predicted LTL was associated with both recurrence and survival. Dichotomized at the median value of GRS, patients with low GRS (indicating short LTL) exhibited significantly increased risks of recurrence (HR=1.26, 95% CI, 1.03-1.54, P=0.025) and death (HR=1.23, 95% CI, 1.00-1.50, P=0.045). Hence, we concluded that genetically predicted short LTL is associated with worse prognosis in RCC patients.

Indexed as

genetic risk score (GRS)leukocyte telomere lengthMendelian randomizationrecurrenceRenal cell carcinomasurvival

Identifiers

PMID33163281
PMCPMC7642657
OpenAlexW3101047924

What OpenQuestion holds

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Registered trials

None linked

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.