Evidence map›Paper›PMID 31183974›Full record

ArticleCancer medicine2019

Low level of Cyclin-D1 correlates with worse prognosis of clear cell renal cell carcinoma patients.

Qing-Shui Wang, Feng Li, Zi-Qiang Liao, Ke Li, Xin-Liu Yang, You-Yu Lin, Yi-Lin Zhao, Shu-Yun Weng, Yun Xia, Yan Ye and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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

13 authors at 2 institutions in 1 country.

Qing-Shui WangProvincial University Key Laboratory of Cellular Stress Response and Metabolic Regulation, Key Laboratory of Opto Electronic Science and Technology for Medicine of Ministry of Education, College of Life Sciences, Fujian Normal University, Fuzhou, P.R. China.
Feng LiDepartment of Pathology, Provincial Clinical Medical College of Fujian Medical University, Fuzhou, P.R. China.
Zi-Qiang LiaoProvincial University Key Laboratory of Cellular Stress Response and Metabolic Regulation, Key Laboratory of Opto Electronic Science and Technology for Medicine of Ministry of Education, College of Life Sciences, Fujian Normal University, Fuzhou, P.R. China.
Ke LiProvincial University Key Laboratory of Cellular Stress Response and Metabolic Regulation, Key Laboratory of Opto Electronic Science and Technology for Medicine of Ministry of Education, College of Life Sciences, Fujian Normal University, Fuzhou, P.R. China.
Xin-Liu YangProvincial University Key Laboratory of Cellular Stress Response and Metabolic Regulation, Key Laboratory of Opto Electronic Science and Technology for Medicine of Ministry of Education, College of Life Sciences, Fujian Normal University, Fuzhou, P.R. China.
You-Yu LinProvincial University Key Laboratory of Cellular Stress Response and Metabolic Regulation, Key Laboratory of Opto Electronic Science and Technology for Medicine of Ministry of Education, College of Life Sciences, Fujian Normal University, Fuzhou, P.R. China.
Yi-Lin ZhaoProvincial University Key Laboratory of Cellular Stress Response and Metabolic Regulation, Key Laboratory of Opto Electronic Science and Technology for Medicine of Ministry of Education, College of Life Sciences, Fujian Normal University, Fuzhou, P.R. China.
Shu-Yun WengProvincial University Key Laboratory of Cellular Stress Response and Metabolic Regulation, Key Laboratory of Opto Electronic Science and Technology for Medicine of Ministry of Education, College of Life Sciences, Fujian Normal University, Fuzhou, P.R. China.
Yun XiaProvincial University Key Laboratory of Cellular Stress Response and Metabolic Regulation, Key Laboratory of Opto Electronic Science and Technology for Medicine of Ministry of Education, College of Life Sciences, Fujian Normal University, Fuzhou, P.R. China.
Yan YeProvincial University Key Laboratory of Cellular Stress Response and Metabolic Regulation, Key Laboratory of Opto Electronic Science and Technology for Medicine of Ministry of Education, College of Life Sciences, Fujian Normal University, Fuzhou, P.R. China.
Su-Huan LiProvincial University Key Laboratory of Cellular Stress Response and Metabolic Regulation, Key Laboratory of Opto Electronic Science and Technology for Medicine of Ministry of Education, College of Life Sciences, Fujian Normal University, Fuzhou, P.R. China.
Chen-Yi WangProvincial University Key Laboratory of Cellular Stress Response and Metabolic Regulation, Key Laboratory of Opto Electronic Science and Technology for Medicine of Ministry of Education, College of Life Sciences, Fujian Normal University, Fuzhou, P.R. China.
Yao LinProvincial University Key Laboratory of Cellular Stress Response and Metabolic Regulation, Key Laboratory of Opto Electronic Science and Technology for Medicine of Ministry of Education, College of Life Sciences, Fujian Normal University, Fuzhou, P.R. China.ORCID 0000-0002-0493-0155
Fujian Normal University · CNFujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cyclin-D1 (CCND1) belongs to the highly conserved cyclin family whose members are characterized by abundant expression during the cell cycle. As an oncogene, high level of CCND1 was observed and related to poor prognosis and tumor recurrence in many cancers. In this study, we focused on the role of CCND1 in the clinical outcome of clear cell renal cell carcinoma (ccRCC). Gene Expression Omnibus database, The Cancer Genome Atlas database, and immunohistochemical staining were used. The mRNA and protein levels of CCND1 were significantly enhanced in ccRCC tumor tissues. However, the low level of CCND1, but not high level of CCND1, was related to poor prognosis and tumor recurrence in ccRCC. Further analysis showed that CCND1 mRNA level decreased with increasing ccRCC tumor grades and the rate of recurrence in ccRCC patients. In a nomogram model, the CCND1 mRNA level was shown to help predict ccRCC patient recurrence. CCND1 is a strong determinant for prediction of recurrence. The patients with high CCND1 level appear to have a more favorable prognosis together with more frequent low-grade tumors and low rate of recurrence. This is the first study to investigate the prognostic roles of CCND1 in ccRCC and discovered that CCND1 had an unconventional positive impact on the clinical outcome of ccRCC patients.

Indexed as

Down-RegulationBiomarkers, TumorCarcinoma, Renal CellCyclin D1FemaleGene Expression Regulation, NeoplasticHumansKidney NeoplasmsMaleNeoplasm GradingNeoplasm Recurrence, LocalNomogramsPrognosisBiomarkers, TumorCCND1 protein, humanCyclin D1clear cell renal cell carcinomaCyclin-D1gradeprognosisrecurrence

Identifiers

PMID31183974
PMCPMC6675723
OpenAlexW2952400124

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.