Evidence map›Paper›PMID 36354714›Full record

SynthesisCurrent oncology (Toronto, Ont.)2022

PD-L1 Activity Is Associated with Partial EMT and Metabolic Reprogramming in Carcinomas.

Srinath Muralidharan, Manas Sehgal, R Soundharya, Susmita Mandal, Sauma Suvra Majumdar, M Yeshwanth, Aryamaan Saha, Mohit Kumar Jolly

Abstract readMeta-Analysis
In one paragraph

Synthesis in Current oncology (Toronto, Ont.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Review
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  4. Clinical and molecular characterization ofJournal for immunotherapy of cancer · 2025
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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

8 authors.

Srinath MuralidharanCentre for BioSystems Science and Engineering, Indian Institute of Science, Bangalore 560012, India.
Manas SehgalCentre for BioSystems Science and Engineering, Indian Institute of Science, Bangalore 560012, India.ORCID 0000-0002-1126-9481
R SoundharyaCentre for BioSystems Science and Engineering, Indian Institute of Science, Bangalore 560012, India.
Susmita MandalCentre for BioSystems Science and Engineering, Indian Institute of Science, Bangalore 560012, India.
Sauma Suvra MajumdarDepartment of Biotechnology, National Institute of Technology, Durgapur 713216, India.
M YeshwanthCentre for BioSystems Science and Engineering, Indian Institute of Science, Bangalore 560012, India.
Aryamaan SahaDepartment of Biotechnology, Indian Institute of Technology Madras, Chennai 600036, India.ORCID 0000-0002-4497-9631
Mohit Kumar JollyCentre for BioSystems Science and Engineering, Indian Institute of Science, Bangalore 560012, India.ORCID 0000-0002-6631-2109

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune evasion and metabolic reprogramming are hallmarks of cancer progression often associated with a poor prognosis and frequently present significant challenges for cancer therapies. Recent studies have highlighted the dynamic interaction between immunosuppression and the dysregulation of energy metabolism in modulating the tumor microenvironment to promote cancer aggressiveness. However, a pan-cancer association among these two hallmarks, and a potent common driver for them-epithelial-mesenchymal transition (EMT)-remains to be done. This meta-analysis across 184 publicly available transcriptomic datasets as well as The Cancer Genome Atlas (TCGA) data reveals that an enhanced PD-L1 activity signature along with other immune checkpoint markers correlate positively with a partial EMT and an elevated glycolysis signature but a reduced OXPHOS signature in many carcinomas. These trends were also recapitulated in single-cell, RNA-seq, time-course EMT induction data across cell lines. Furthermore, across multiple cancer types, concurrent enrichment of glycolysis and PD-L1 results in worse outcomes in terms of overall survival as compared to enrichment for only PD-L1 activity or expression. These results highlight potential functional synergy among these interconnected axes of cellular plasticity in enabling metastasis and multi-drug resistance in cancer.

Indexed as

B7-H1 AntigenCarcinomaEpithelial-Mesenchymal TransitionHumansPrognosisTumor MicroenvironmentB7-H1 Antigenglycolysisimmune checkpoint moleculesmeta-analysismetabolic plasticityoxidative phosphorylationpartial EMT

Identifiers

PMID36354714
PMCPMC9688938

What OpenQuestion holds

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Registered trials

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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.