Evidence map›Paper›PMID 34529197›Full record

ArticleBreast cancer research and treatment2021

Hyperglycemic conditions proliferate triple negative breast cancer cells: role of ornithine decarboxylase.

Caleb C Capellen, Jose Ortega-Rodas, M Jane Morwitzer, Hadassha M N Tofilau, Matthew Dunworth, Robert A Casero, Surabhi Chandra

Open access · greenAbstract read
In one paragraph

Article in Breast cancer research and treatment, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Caleb C CapellenDepartment of Biology, University of Nebraska-Kearney, 2401 W. 11th Ave, BHS335, Kearney, NE, 68849, USA.
Jose Ortega-RodasDepartment of Biology, University of Nebraska-Kearney, 2401 W. 11th Ave, BHS335, Kearney, NE, 68849, USA.
M Jane MorwitzerDepartment of Biology, University of Nebraska-Kearney, 2401 W. 11th Ave, BHS335, Kearney, NE, 68849, USA.
Hadassha M N TofilauDepartment of Biology, University of Nebraska-Kearney, 2401 W. 11th Ave, BHS335, Kearney, NE, 68849, USA.
Matthew DunworthThe Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Bunting/Blaustein Cancer Research Building 1 1650 Orleans Street - Room 551, Baltimore, MD, 21231, USA.
Robert A CaseroThe Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Bunting/Blaustein Cancer Research Building 1 1650 Orleans Street - Room 551, Baltimore, MD, 21231, USA.
Surabhi ChandraDepartment of Biology, University of Nebraska-Kearney, 2401 W. 11th Ave, BHS335, Kearney, NE, 68849, USA. chandras2@unk.edu.ORCID http://orcid.org/0000-0003-1403-2911
University of Nebraska at Kearney · USJohns Hopkins University · US

Funding

UNMC Structural Biology CoreP20GM103427 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI PAUL L SORGEN · 2012 to 2026
$59.2M
Identification of novel spermine oxidase (SMOX) inhibitors as probes for an emerging chemoprevention targetR01CA204345 · NCI · JOHNS HOPKINS UNIVERSITY · PI CASERO, ROBERT A., WOSTER, PATRICK M · 2016 to 2020
$3.4M
Self-immolative prodrug/miRNA nanoparticle combinations for cancer treatmentR01CA235863 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI CASERO, ROBERT A., OUPICKY, DAVID · 2019 to 2023
$2.3M
Division of Cancer Prevention, National Cancer Institute CA204345Division of Cancer Prevention, National Cancer Institute CA235863NCI NIH HHS R01 CA204345NCI NIH HHS R01 CA235863NIGMS NIH HHS GM103427NIGMS NIH HHS P20 GM103427
6 · The paper itself

Abstract

purposeSeveral cancer subtypes (pancreatic, breast, liver, and colorectal) rapidly advance to higher aggressive stages in diabetes. Though hyperglycemia has been considered as a fuel for growth of cancer cells, pathways leading to this condition are still under investigation. Cellular polyamines can modulate normal and cancer cell growth, and inhibitors of polyamine synthesis have been approved for treating colon cancer, however the role of polyamines in diabetes-mediated cancer advancement is unclear as yet. We hypothesized that polyamine metabolic pathway is involved with increased proliferation of breast cancer cells under high glucose (HG) conditions.

methodsStudies were performed with varying concentrations of glucose (5-25 mM) exposure in invasive, triple negative breast cancer cells, MDA-MB-231; non-invasive, estrogen/progesterone receptor positive breast cancer cells, MCF-7; and non-tumorigenic mammary epithelial cells, MCF-10A.

resultsThere was a significant increase in proliferation with HG (25 mM) at 48-72 h in both MDA-MB-231 and MCF-10A cells but no such effect was observed in MCF-7 cells. This was correlated to higher activity of ornithine decarboxylase (ODC), a rate-limiting enzyme in polyamine synthesis pathway. Inhibitor of polyamine synthesis (difluoromethylornithine, DFMO, 5 mM) was quite effective in suppressing HG-mediated cell proliferation and ODC activity in MDA-MB-231 and MCF-10A cells. Polyamine (putrescine) levels were significantly elevated with HG treatment in MDA-MB-231 cells. HG exposure also increased the metastasis of MDA-MB-231 cells.

conclusionsOur cellular findings indicate that polyamine inhibition should be explored in patient population as a target for future chemotherapeutics in diabetic breast cancer.

Indexed as

Breast NeoplasmsHyperglycemiaTriple Negative Breast NeoplasmsEflornithineFemaleHumansOrnithine DecarboxylaseOrnithine Decarboxylase InhibitorsPutrescineEflornithineOrnithine DecarboxylaseOrnithine Decarboxylase InhibitorsPutrescineBreast cancerDiabetesHigh glucoseOrnithine decarboxylasePolyaminePutrescine

Identifiers

PMID34529197
PMCPMC8638560
OpenAlexW3168885611

What OpenQuestion holds

Textmetadata
LicenceTDM
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.