Evidence map›Paper›PMID 34298999›Full record

ReviewInternational journal of molecular sciences2021

Cisplatin Resistance and Redox-Metabolic Vulnerability: A Second Alteration.

Medhi Wangpaichitr, George Theodoropoulos, Dan J M Nguyen, Chunjing Wu, Sydney A Spector, Lynn G Feun, Niramol Savaraj

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  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

7 authors at 2 institutions in 1 country.

Medhi WangpaichitrDepartment of Veterans Affairs, Miami VA Healthcare System, Research Service (151), Miami, FL 33125, USA.
George TheodoropoulosDepartment of Veterans Affairs, Miami VA Healthcare System, Research Service (151), Miami, FL 33125, USA.
Dan J M NguyenDepartment of Veterans Affairs, Miami VA Healthcare System, Research Service (151), Miami, FL 33125, USA.
Chunjing WuDepartment of Veterans Affairs, Miami VA Healthcare System, Research Service (151), Miami, FL 33125, USA.
Sydney A SpectorDepartment of Veterans Affairs, Miami VA Healthcare System, Research Service (151), Miami, FL 33125, USA.
Lynn G FeunDepartment of Medicine, Hematology/Oncology, Miller School of Medicine, University of Miami, Miami, FL 33136, USA.
Niramol SavarajDepartment of Medicine, Hematology/Oncology, Miller School of Medicine, University of Miami, Miami, FL 33136, USA.
Miami VA Healthcare System · USUniversity of Miami · US

Funding

Hi-jacking the kynurenine pathway: A new therapeutic approach used to treat cisplatin resistant lung cancer that evades immune surveillance and proliferates with increased ROS levelsI01BX004371 · VA · MIAMI VA HEALTH CARE SYSTEM · PI WANGPAICHITR, MEDHI · 2018 to 2025
–
Metabolic reprogramming: A new paradigm for targeting cisplatin resistant cellsIK2BX001289 · VA · MIAMI VA HEALTH CARE SYSTEM · PI WANGPAICHITR, MEDHI · 2013 to 2017
–
BLRD VA I01 BX004371BLRD VA I01 BX005051BLRD VA IK2 BX001289U.S. Department of Veterans Affairs 1BX003328U.S. Department of Veterans Affairs 1I01BX004371
6 · The paper itself

Abstract

The development of drug resistance in tumors is a major obstacle to effective cancer chemotherapy and represents one of the most significant complications to improving long-term patient outcomes. Despite early positive responsiveness to platinum-based chemotherapy, the majority of lung cancer patients develop resistance. The development of a new combination therapy targeting cisplatin-resistant (CR) tumors may mark a major improvement as salvage therapy in these patients. The recent resurgence in research into cellular metabolism has again confirmed that cancer cells utilize aerobic glycolysis ("the Warburg effect") to produce energy. Hence, this observation still remains a characteristic hallmark of altered metabolism in certain cancer cells. However, recent evidence promotes another concept wherein some tumors that acquire resistance to cisplatin undergo further metabolic alterations that increase tumor reliance on oxidative metabolism (OXMET) instead of glycolysis. Our review focuses on molecular changes that occur in tumors due to the relationship between metabolic demands and the importance of NAD

Indexed as

Drug Resistance, NeoplasmCisplatinEnergy MetabolismGlycolysisHumansKynurenineMitochondriaNADNeoplasmsOxidation-ReductionPoly (ADP-Ribose) Polymerase-1Reactive Oxygen SpeciesSirtuinsTumor MicroenvironmentCisplatinKynurenineNADPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1Reactive Oxygen SpeciesSirtuinscisplatin resistancemetabolismoxidative metabolismreactive oxygen species

Identifiers

PMID34298999
PMCPMC8304747
OpenAlexW3182391099

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.