Evidence map›Paper›PMID 26735579›Full record

ArticleOncotarget2016

RPS7 inhibits colorectal cancer growth via decreasing HIF-1α-mediated glycolysis.

Wen Zhang, Duo Tong, Fei Liu, Dawei Li, Jiajia Li, Xi Cheng, Ziliang Wang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

31 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

7 authors at 2 institutions in 1 country.

Wen ZhangCancer Institute and Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Duo TongCancer Institute and Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Fei LiuDepartment of Gynecological Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Dawei LiDepartment of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Jiajia LiDepartment of Gynecological Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Xi ChengDepartment of Gynecological Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Ziliang WangCancer Institute and Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Fudan University Shanghai Cancer Center · CNShanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ribosomal protein S7 (RPS7) acts as a tumor suppressor in primary tumorigenesis but its role in cancer metabolism remains unclear. In this study, we demonstrate that RPS7 inhibits the colorectal cancer (CRC) cell glycolysis by suppressing the expression of hypoxia-inducible transcription factor-1α (HIF-1α) and the metabolic promoting proteins glucose transporter 4 (GLUT4) and lactate dehydrogenase B (LDHB). Further study found that the enhanced expression of HIF-1α abrogates the overexpression effects of RPS7 on CRC. In vivo assays also demonstrate that RPS7 suppresses colorectal cancer tumorigenesis and glycolysis. Clinically, the tissue microarray (TMA) analysis discloses the negative regulatory association between RPS7 and HIF-1α in colorectal cancer. Meanwhile, overexpression of RPS7 in colorectal cancer tissues predicts good overall survival and progression-free survival, but high expression level of HIF-1α indicates poor overall survival and progression-free survival. Overall, we reveal that RPS7 inhibits colorectal cancer glycolysis through HIF-1α-associated signaling and may be a promising biomarker for prognosis prediction and a potential target for therapeutic treatment.

Indexed as

GlycolysisAdenocarcinomaAdenocarcinoma, MucinousAdultAgedAnimalsApoptosisCell ProliferationColorectal NeoplasmsFemaleGlucose Transporter Type 4HumansHypoxia-Inducible Factor 1, alpha SubunitImmunoenzyme TechniquesLactate DehydrogenasesMaleD-lactate dehydrogenaseGlucose Transporter Type 4HIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitLactate DehydrogenasesRibosomal Proteinsribosomal protein S7RNA, MessengerSLC2A4 protein, humanCRCglycolysisHIF-1αproliferationRPS7

Identifiers

PMID26735579
PMCPMC4868722
OpenAlexW2282865274

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.