Evidence map›Paper›PMID 37413991›Full record

ArticleCell metabolism2023

Immunometabolic coevolution defines unique microenvironmental niches in ccRCC.

Cerise Tang, Amy X Xie, Eric Minwei Liu, Fengshen Kuo, Minsoo Kim, Renzo G DiNatale, Mahdi Golkaram, Ying-Bei Chen, Sounak Gupta, Robert J Motzer and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Cell metabolism, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Lactate-Driven IL8+ Tumor-Associated Macrophages Mediate Immunosuppression and Resistance to Immunotherapy in Clear-Cell Renal Cell Carcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  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

20 authors at 2 institutions in 1 country.

Cerise TangComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Physiology, Biophysics and Systems Biology Graduate Program, Weill Cornell Medicine, New York, NY, USA.
Amy X XieComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Biochemistry, Structural Biology, Cell Biology, Developmental Biology and Molecular Biology Graduate Program, Weill Cornell Medicine, New York, NY, USA.
Eric Minwei LiuComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Fengshen KuoUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Minsoo KimComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Renzo G DiNataleComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Mahdi GolkaramIllumina, Inc., 5200 Illumina Way, San Diego, CA 92122, USA.
Ying-Bei ChenDepartment of Pathology, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Sounak GuptaDepartment of Pathology, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Robert J MotzerGenitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Paul RussoUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Jonathan ColemanUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Maria I CarloGenitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Martin H VossGenitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Ritesh R KotechaGenitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Chung-Han LeeDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Wesley TanseyComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Nikolaus SchultzComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
A Ari HakimiUrology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. Electronic address: hakimia@mskcc.org.
Ed ReznikComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. Electronic address: reznike@mskcc.org.
Memorial Sloan Kettering Cancer Center · USIllumina (United States) · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
The Center for Tumor-Immune Systems Biology at MSKCCU54CA274492 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Christina S Leslie · 2022 to 2026
$16.3M
Defining the function of Complex I truncating mutations in cancerR37CA276200 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Payam Gammage, Eduard Reznik · 2023 to 2026
$2.5M
Macrophages as modulators of T cell function and therapeutic response in clear cell renal cell carcinomaR01CA258886 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI HAKIMI, ABRAHAM ARI · 2021 to 2025
$2.4M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA258886NCI NIH HHS R37 CA276200NCI NIH HHS U54 CA274492
6 · The paper itself

Abstract

Tumor cell phenotypes and anti-tumor immune responses are shaped by local metabolite availability, but intratumoral metabolite heterogeneity (IMH) and its phenotypic consequences remain poorly understood. To study IMH, we profiled tumor/normal regions from clear cell renal cell carcinoma (ccRCC) patients. A common pattern of IMH transcended all patients, characterized by correlated fluctuations in the abundance of metabolites and processes associated with ferroptosis. Analysis of intratumoral metabolite-RNA covariation revealed that the immune composition of the microenvironment, especially the abundance of myeloid cells, drove intratumoral metabolite variation. Motivated by the strength of RNA-metabolite covariation and the clinical significance of RNA biomarkers in ccRCC, we inferred metabolomic profiles from the RNA sequencing data of ccRCC patients enrolled in 7 clinical trials, and we ultimately identifyied metabolite biomarkers associated with response to anti-angiogenic agents. Local metabolic phenotypes, therefore, emerge in tandem with the immune microenvironment, influence ongoing tumor evolution, and are associated with therapeutic sensitivity.

Indexed as

CarcinomaCarcinoma, Renal CellKidney NeoplasmsBiomarkers, TumorHumansMyeloid CellsRNATumor MicroenvironmentBiomarkers, TumorRNAcancer metabolismimmune microenvironmentimmunometabolismimputationintratumoral heterogeneitymetabolitesmetabolomicsrenal cell carcinomatranscriptomics

Identifiers

PMID37413991
PMCPMC10603615
OpenAlexW4383217822

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.