Evidence map›Paper›PMID 30151352›Full record

ReviewFrontiers in oncology2018

Metabolic Switch in the Tumor Microenvironment Determines Immune Responses to Anti-cancer Therapy.

Barbara Wegiel, Marta Vuerich, Saeed Daneshmandi, Pankaj Seth

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

73 citing papers in PubMed, 130 citations in OpenAlex.

  1. Article
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  10. Microenvironment-based immunotherapy in oral cancer: a comprehensive review.Medical oncology (Northwood, London, England) · 2025
    Review
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13 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

4 authors at 2 institutions in 1 country.

Barbara WegielDepartment of Surgery, Beth Israel Deaconess Medical Center, Boston, MA, United States.
Marta VuerichDivision of Interdisciplinary Medicine, Beth Israel Deaconess Medical Center, Boston, MA, United States.
Saeed DaneshmandiDivision of Interdisciplinary Medicine, Beth Israel Deaconess Medical Center, Boston, MA, United States.
Pankaj SethCancer Research Institute, Beth Israel Deaconess Medical Center, Boston, MA, United States.
Beth Israel Deaconess Medical Center · USCancer Research Institute · US

Funding

Role of biliverdin reductase during sterile inflammation in the liver.R01DK104714 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI WEGIEL, BARBARA · 2016 to 2020
$2.0M
Hyperpolarized NMR for Studies of Cancer Therapies Targeting the Warburg EffectR01CA169470 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI GRANT, AARON KEITH · 2013 to 2017
$1.8M
Heme degradation pathway and immunomodulation in prostate cancer.R21CA169904 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI WEGIEL, BARBARA · 2013 to 2014
$411k
NCI NIH HHS R01 CA169470NCI NIH HHS R21 CA169904NIDDK NIH HHS R01 DK104714
6 · The paper itself

Abstract

Tumor-induced immune tolerance permits growth and spread of malignant cells. Cancer cells have strong influence on surrounding cells and shape the hypoxic tumor microenvironment (TME) facilitating cancer progression. A dynamic change in glucose metabolism occurring in cancer cells and its influence on the TME are still poorly understood. Indeed, cancer and/or immune cells undergo rapid adaptation in metabolic pathways during cancer progression. Metabolic reprograming affects macrophages, T cells, and myeloid derived suppressor cells (MDSCs) among other immune cells. Their role in the TME depends on a nature and concentration of factors, such as cytokines, reactive oxygen species (ROS), growth factors, and most importantly, diffusible metabolites (i.e., lactate). Further, the amounts of available nutrients and oxygen as well as activity of microbiota may influence metabolic pathways in the TME. The roles of metabolites in regulating of the interaction between immune and cancer cell are highlighted in this review. Targeting metabolic reprogramming or signaling pathways controlling cell metabolism in the TME might be a potential strategy for anti-cancer therapy alone or in combination with current immunotherapies.

Indexed as

HIF-1αimmune stromalactatemetabolic reprogrammingtumor microenvironment (TME)

Identifiers

PMID30151352
PMCPMC6099109
OpenAlexW2885086490

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.