Evidence map›Paper›PMID 33673398›Full record

ReviewCancers2021

Oxidative Stress in the Tumor Microenvironment and Its Relevance to Cancer Immunotherapy.

Nada S Aboelella, Caitlin Brandle, Timothy Kim, Zhi-Chun Ding, Gang Zhou

Abstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 148 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
148citing papers in PubMed, 1 pooled it
–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

148 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Immunomodulatory Nanozymes as Programmable Redox-Immune Set-Point Regulators.Small (Weinheim an der Bergstrasse, Germany) · 2026
    Review
  6. On the Edge of Benefit and Harm: Reactive Oxygen Species in Cancer.International journal of molecular sciences · 2026
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Crosstalk BetweenCancers · 2026
    Review
  18. Article
  19. Review
  20. Article

88 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

5 authors.

Nada S AboelellaGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0002-9009-9897
Caitlin BrandleGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.
Timothy KimThe Center for Undergraduate Research and Scholarship, Augusta University, Augusta, GA 30912, USA.
Zhi-Chun DingGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.ORCID 0000-0001-6322-8641
Gang ZhouGeorgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.

Funding

Exploiting the immunomodulatory effects of sulindac and novel non-COX inhibitory derivatives for cancer treatmentR01CA238514 · NCI · AUGUSTA UNIVERSITY · PI PIAZZA, GARY A, ZHOU, GANG · 2020 to 2024
$2.1M
Chemotherapy-induced MDSCs and antitumor immunityR01CA215523 · NCI · AUGUSTA UNIVERSITY · PI ZHOU, GANG · 2017 to 2021
$1.7M
NCI NIH HHS 1R01CA215523; 1R01CA238514NCI NIH HHS R01 CA215523NCI NIH HHS R01 CA238514
6 · The paper itself

Abstract

It has been well-established that cancer cells are under constant oxidative stress, as reflected by elevated basal level of reactive oxygen species (ROS), due to increased metabolism driven by aberrant cell growth. Cancer cells can adapt to maintain redox homeostasis through a variety of mechanisms. The prevalent perception about ROS is that they are one of the key drivers promoting tumor initiation, progression, metastasis, and drug resistance. Based on this notion, numerous antioxidants that aim to mitigate tumor oxidative stress have been tested for cancer prevention or treatment, although the effectiveness of this strategy has yet to be established. In recent years, it has been increasingly appreciated that ROS have a complex, multifaceted role in the tumor microenvironment (TME), and that tumor redox can be targeted to amplify oxidative stress inside the tumor to cause tumor destruction. Accumulating evidence indicates that cancer immunotherapies can alter tumor redox to intensify tumor oxidative stress, resulting in ROS-dependent tumor rejection. Herein we review the recent progresses regarding the impact of ROS on cancer cells and various immune cells in the TME, and discuss the emerging ROS-modulating strategies that can be used in combination with cancer immunotherapies to achieve enhanced antitumor effects.

Indexed as

immunotherapyoxidative stressreactive oxygen speciestumor microenvironment

Identifiers

PMID33673398
PMCPMC7956301

What OpenQuestion holds

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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.