Evidence map›Paper›PMID 28969010›Full record

ArticleOncotarget2017

Dual inhibition of glycolysis and glutaminolysis as a therapeutic strategy in the treatment of ovarian cancer.

Li Sun, Yajie Yin, Leslie H Clark, Wenchuan Sun, Stephanie A Sullivan, Arthur-Quan Tran, Jianjun Han, Lu Zhang, Hui Guo, Esther Madugu and 7 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
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  4. Article
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  7. Article
  8. Review
  9. Article
  10. Insulin and cancer: a tangled web.The Biochemical journal · 2022
    Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Development of a RapidACS omega · 2021
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Potential Applications of NRF2 Modulators in Cancer Therapy.Antioxidants (Basel, Switzerland) · 2020
    Review
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

17 authors at 5 institutions in 2 countries.

Li Sun *Department of Gynecologic Oncology, Shandong Cancer Hospital Affiliated to Shandong University, Shandong Academy of Medical Sciences, Jinan, Shandong Province, People's Republic of China.
Yajie Yin *Department of Gynecologic Oncology, Shandong Cancer Hospital Affiliated to Shandong University, Shandong Academy of Medical Sciences, Jinan, Shandong Province, People's Republic of China.
Leslie H ClarkDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Wenchuan SunDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Stephanie A SullivanDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Arthur-Quan TranDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Jianjun HanDepartment of Surgical Oncology, Shandong Cancer Hospital Affiliated to Shandong University, Shandong Academy of Medical Sciences, Jinan, Shandong Province, People's Republic of China.
Lu ZhangDepartment of Gynecologic Oncology, Shandong Cancer Hospital Affiliated to Shandong University, Shandong Academy of Medical Sciences, Jinan, Shandong Province, People's Republic of China.
Hui GuoDepartment of Gynecologic Oncology, Shandong Cancer Hospital Affiliated to Shandong University, Shandong Academy of Medical Sciences, Jinan, Shandong Province, People's Republic of China.
Esther MaduguDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Tommy PanDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Amanda L JacksonDivision of Gynecologic Oncology, University of Cincinnati, Cincinnati, OH, USA.
Joshua KilgoreHouston Methodist Gynecologic Oncology Associates, Houston, TX, USA.
Hannah M JonesDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Timothy P GilliamDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Chunxiao ZhouDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Victoria L Bae-JumpDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
University of North Carolina at Chapel Hill · USShandong University · CNHouston Methodist · USShandong Tumor Hospital · CNUniversity of Cincinnati · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI David Darr · 1985 to 2026
$201.5M
UNC Clinical Translation Science Award-K12 Scholars Program (KL2)KL2RR025746 · NCRR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RUNGE, MARSCHALL S. · 2008 to 2011
$9.0M
NCI NIH HHS P30 CA016086NCRR NIH HHS KL2 RR025746
6 · The paper itself

Abstract

Cancer cell metabolism is required to support the biosynthetic demands of cell growth and cell division, and to maintain reduction oxidaton (redox) homeostasis. This study was designed to test the effects of glucose and glutamine on ovarian cancer cell growth and explore the inter-relationship between glycolysis and glutaminolysis. The SKOV3, IGROV-1 and Hey ovarian cancer cell lines were assayed for glucose, pyruvate and glutamine dependence by analyzing cytotoxicity, cell cycle progression, apoptosis and ATP production. As determined by MTT assay, glucose stimulated cell growth while the combination of glucose, glutamine and pyruvate resulted in the greatest stimulation of cell proliferation. Furthermore, 2-deoxy-glucose (2-DG) and 3-bromopyruvate (3-BP) induced apoptosis, caused G1 phase cell cycle arrest and reduced glycolytic activity. Moreover, 2-DG in combination with a low dose of aminooxyacetate (AOA) synergistically increased the sensitivity to 2-DG in the inhibition of cell growth in the ovarian cancer cell lines. These studies suggest that dual inhibition of glycolysis and glutaminolysis may be a promising therapeutic strategy for the treatment of ovarian cancer.

Indexed as

AMPK/mTORglutaminolysisglycolysisovarian cancer

Identifiers

PMID28969010
PMCPMC5609942
OpenAlexW2724377172

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.