Evidence map›Paper›PMID 28951458›Full record

ArticleCancer research2017

PHGDH as a Key Enzyme for Serine Biosynthesis in HIF2α-Targeting Therapy for Renal Cell Carcinoma.

Hirofumi Yoshino, Nijiro Nohata, Kazutaka Miyamoto, Masaya Yonemori, Takashi Sakaguchi, Satoshi Sugita, Toshihiko Itesako, Satoshi Kofuji, Masayuki Nakagawa, Rajvir Dahiya and 1 more

Abstract read
In one paragraph

Article in Cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
–field-weighted citation impact
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

61 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. PHGDH is a targetable driver of PDAC progression.bioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Belzutifan for the treatment of renal cell carcinoma.Therapeutic advances in medical oncology · 2025
    Review
  17. Article
  18. Article
  19. Article
  20. PHGDH: a novel therapeutic target in cancer.Experimental & molecular medicine · 2024
    Review

1 more citing papers are in PubMed but not listed here.

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

11 authors.

Hirofumi YoshinoDepartment of Urology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Nijiro NohataMoores Cancer Center, University of California, San Diego, California.
Kazutaka MiyamotoDepartment of Urology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Masaya YonemoriDepartment of Urology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Takashi SakaguchiDepartment of Urology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Satoshi SugitaDepartment of Urology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Toshihiko ItesakoDepartment of Urology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Satoshi KofujiDepartment of Physiological Chemistry, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Masayuki NakagawaDepartment of Urology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Rajvir DahiyaDepartment of Urology, VA Medical Center and UCSF, San Francisco, California. enokida@m.kufm.kagoshima-u.ac.jp rdahiya@urology.ucsf.edu.
Hideki EnokidaDepartment of Urology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan. enokida@m.kufm.kagoshima-u.ac.jp rdahiya@urology.ucsf.edu.

Funding

Molecular biomarkers for kidney cancer prognosis using non-coding RNAsR01CA199694 · NCI · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI TANAKA, YUICHIRO · 2016 to 2020
$1.7M
BLRD VA I01 BX001123BLRD VA IK6 BX004473NCI NIH HHS R01 CA199694
6 · The paper itself

Abstract

Continuous activation of hypoxia-inducible factor (HIF) is important for progression of renal cell carcinoma (RCC) and acquired resistance to antiangiogenic multikinase and mTOR inhibitors. Recently, HIF2α antagonists PT2385 and PT2399 were developed and are being evaluated in a phase I clinical trial for advanced or metastatic clear cell RCC (ccRCC). However, resistance to HIF2α antagonists would be expected to develop. In this study, we identified signals activated by HIF2α deficiency as candidate mediators of resistance to the HIF2α antagonists. We established sunitinib-resistant tumor cells

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCarcinoma, Renal CellCell Line, TumorCRISPR-Cas SystemsEndothelial PAS Domain-Containing Protein 1Enzyme InhibitorsFemaleGene Expression Regulation, NeoplasticHumansIndansKidney NeoplasmsMice, Inbred BALB CMice, NudeMolecular Targeted TherapyPhosphoglycerate DehydrogenaseBasic Helix-Loop-Helix ProteinsEndothelial PAS Domain-Containing Protein 1Enzyme InhibitorsIndansPhosphoglycerate DehydrogenasePT2385PT2399SerineSulfones

Identifiers

PMID28951458
PMCPMC5893502

What OpenQuestion holds

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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.