Evidence map›Paper›PMID 27595393›Full record

ArticleNature2016

On-target efficacy of a HIF-2α antagonist in preclinical kidney cancer models.

Hyejin Cho, Xinlin Du, James P Rizzi, Ella Liberzon, Abhishek A Chakraborty, Wenhua Gao, Ingrid Carvo, Sabina Signoretti, Richard K Bruick, John A Josey and 2 more

Open access · greenAbstract read
In one paragraph

Article in Nature, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 310 papers.

0numbers the graph read from it
0cells of the map it votes in
310citing papers in PubMed
18.7field-weighted citation impact, top 1% 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

310 citing papers in PubMed, 448 citations in OpenAlex.

  1. Randomized phase II dose comparison LITESPARK-013 study of belzutifan in patients with advanced clear cell renal cell carcinoma.Annals of oncology : official journal of the European Society for Medical Oncology · 2024
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  10. The clinical landscape of HIF2α inhibitors in oncology.Nature reviews. Clinical oncology · 2026
    Review
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  15. Review
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250 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 1 country.

Hyejin ChoDepartment of Medical Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02215, USA.
Xinlin DuPeloton Therapeutics, Inc., Dallas, Texas 75235, USA.
James P RizziPeloton Therapeutics, Inc., Dallas, Texas 75235, USA.
Ella LiberzonDepartment of Medical Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02215, USA.
Abhishek A ChakrabortyDepartment of Medical Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02215, USA.
Wenhua GaoDepartment of Medical Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02215, USA.
Ingrid CarvoDepartment of Medical Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02215, USA.
Sabina SignorettiDepartment of Medical Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02215, USA.
Richard K BruickDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.
John A JoseyPeloton Therapeutics, Inc., Dallas, Texas 75235, USA.
Eli M WallacePeloton Therapeutics, Inc., Dallas, Texas 75235, USA.
William G KaelinDepartment of Medical Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02215, USA.
Cellerant Therapeutics (United States) · USBrigham and Women's Hospital · USDana-Farber Brigham Cancer Center · USHarvard University · USHoward Hughes Medical Institute · USThe University of Texas Southwestern Medical Center · US

Funding

Treating the P13-Kinase/AKTP50CA101942 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Wanling Xie · 2003 to 2026
$53.4M
The von Hippel-Lindau Tumor Suppressor Gene and Kidney Cancer: Insights into Oxygen Sensing and Treating Cancers Caused by Undruggable MutationsR35CA210068 · NCI · DANA-FARBER CANCER INST · PI WILLIAM G. KAELIN · 2016 to 2026
$10.8M
Howard Hughes Medical InstituteNCI NIH HHS P50 CA101942NCI NIH HHS R35 CA210068
6 · The paper itself

Abstract

Clear cell renal cell carcinoma, the most common form of kidney cancer, is usually linked to inactivation of the pVHL tumour suppressor protein and consequent accumulation of the HIF-2α transcription factor (also known as EPAS1). Here we show that a small molecule (PT2399) that directly inhibits HIF-2α causes tumour regression in preclinical mouse models of primary and metastatic pVHL-defective clear cell renal cell carcinoma in an on-target fashion. pVHL-defective clear cell renal cell carcinoma cell lines display unexpectedly variable sensitivity to PT2399, however, suggesting the need for predictive biomarkers to be developed to use this approach optimally in the clinic.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsBiomarkers, PharmacologicalCarcinoma, Renal CellCell Line, TumorDisease Models, AnimalEndothelial PAS Domain-Containing Protein 1Gene Expression Regulation, NeoplasticHumansIndansKidney NeoplasmsMiceModels, BiologicalNeoplasm MetastasisSulfonesTranscription, GeneticBasic Helix-Loop-Helix ProteinsBiomarkers, PharmacologicalEndothelial PAS Domain-Containing Protein 1IndansPT2399SulfonesVHL protein, mouseVon Hippel-Lindau Tumor Suppressor Protein

Identifiers

PMID27595393
PMCPMC5499381
OpenAlexW2510079645

What OpenQuestion holds

Textmetadata
LicenceTDM
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.