Evidence map›Paper›PMID 35354963›Full record

ArticleActa pharmacologica Sinica2022

ADH1C inhibits progression of colorectal cancer through the ADH1C/PHGDH /PSAT1/serine metabolic pathway.

Sha Li, Hong Yang, Wan Li, Jin-Yi Liu, Li-Wen Ren, Yi-Hui Yang, Bin-Bin Ge, Yi-Zhi Zhang, Wei-Qi Fu, Xiang-Jin Zheng and 2 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.3field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  6. Article
  7. Recent advances in novel targeting mechanisms for colorectal cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Mechanistic study on the inhibition of triple-negative breast cancer progression by LncRNA TFAP2A-AS1 through the regulation of miR-6892/PHGDH.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Article
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  15. Article
  16. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Sha LiThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Hong YangThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Wan LiThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Jin-Yi LiuThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Li-Wen RenThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Yi-Hui YangThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Bin-Bin GeThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Yi-Zhi ZhangThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Wei-Qi FuThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Xiang-Jin ZhengThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China.
Guan-Hua DuThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China. dugh@imm.ac.cn.
Jin-Hua WangThe State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Beijing, 100050, China. wjh@imm.ac.cn.
Chinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is the third most common cancer in men and the second most common cancer in women worldwide. CRC is the second leading cause of cancer-related deaths. Although some progress in the treatment of CRC has been achieved, the molecular mechanism of CRC is still unclear. In this study, alcohol dehydrogenase 1C(ADH1C) was first identified as a target gene closely associated with the development of CRC by the comprehensive application of transcriptomics, proteomics, metabonomics and in silico analysis. The ADH1C mRNA and protein expression in CRC cell lines and tumor tissues was lower than that in normal intestinal epithelial cell lines and healthy tissues. Overexpression of ADH1C inhibited the growth, migration, invasion and colony formation of CRC cell lines and prevented the growth of xenograft tumors in nude mice. The inhibitory effects of ADH1C on CRC cells in vitro were exerted by reducing the expression of PHGDH/PSAT1 and the serine level. This inhibition could be partially reversed by adding serine to the culture medium. These results showed that ADH1C is a potential drug target in CRC.

Indexed as

Alcohol DehydrogenaseColorectal NeoplasmsAnimalsCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMetabolic Networks and PathwaysMiceMice, NudeRNA, MessengerSerineADH1C protein, humanAlcohol DehydrogenaseRNA, MessengerSerineADH1Ccolorectal cancermetabolismPHGDHPSAT1serine

Identifiers

PMID35354963
PMCPMC9525271
OpenAlexW4220693115

What OpenQuestion holds

Textmetadata
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.