Evidence map›Paper›PMID 33036247›Full record

ArticleCancers2020

The Antidiabetic Agent Acarbose Improves Anti-PD-1 and Rapamycin Efficacy in Preclinical Renal Cancer.

Rachael M Orlandella, William J Turbitt, Justin T Gibson, Shannon K Boi, Peng Li, Daniel L Smith, Lyse A Norian

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. 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 1 institution in 2 countries.

Rachael M OrlandellaGraduate Biomedical Sciences, University of Alabama at Birmingham (UAB), Birmingham, AL 35233, USA.ORCID 0000-0002-7572-691X
William J TurbittDepartment of Nutrition Sciences, UAB, Birmingham, AL 35233, USA.
Justin T GibsonGraduate Biomedical Sciences, University of Alabama at Birmingham (UAB), Birmingham, AL 35233, USA.ORCID 0000-0003-2967-5338
Shannon K BoiGraduate Biomedical Sciences, University of Alabama at Birmingham (UAB), Birmingham, AL 35233, USA.
Peng LiSchool of Nursing, UAB, Birmingham, AL 35233, USA.ORCID 0000-0002-9026-9999
Daniel L SmithDepartment of Nutrition Sciences, UAB, Birmingham, AL 35233, USA.
Lyse A NorianGraduate Biomedical Sciences, University of Alabama at Birmingham (UAB), Birmingham, AL 35233, USA.ORCID 0000-0003-1016-313X
University of Alabama at Birmingham · US

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Why is the prevalence of obesity so high in U.S. Southern States? Regional predictors of BMI and obesity treatment response.P30DK056336 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BARBARA A GOWER · 2000 to 2026
$31.9M
IMMUNOLOGIC DISEASES AND BASIC IMMUNOLOGYT32AI007051 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Laurie Ellen Harrington · 1985 to 2026
$13.1M
Identifying outcome mediators of calorie restriction mimetic use in renal cancerR21CA223126 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI NORIAN, LYSE A · 2018 to 2019
$350k
Lumina III System for UAB Optical ImagingS10OD021697 · OD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ZINN, KURT R · 2016 to 2016
$152k
NCI NIH HHS P30 CA013148NIAID NIH HHS T32 AI007051NIDDK NIH HHS P30 DK056336NIH HHS R21CA223126NIH HHS S10 OD021697
6 · The paper itself

Abstract

Although immune checkpoint inhibitors and targeted therapeutics have changed the landscape of treatment for renal cell carcinoma (RCC), most patients do not experience significant clinical benefits. Emerging preclinical studies report that nutrition-based interventions and glucose-regulating agents can improve therapeutic efficacy. However, the impact of such agents on therapeutic efficacy in metastatic kidney cancer remains unclear. Here, we examined acarbose, an alpha-glucosidase inhibitor and antidiabetic agent, in a preclinical model of metastatic kidney cancer. We found that acarbose blunted postprandial blood glucose elevations in lean, nondiabetic mice and impeded the growth of orthotopic renal tumors, an outcome that was reversed by exogenous glucose administration. Delayed renal tumor outgrowth in mice on acarbose occurred in a CD8 T cell-dependent manner. Tumors from these mice exhibited increased frequencies of CD8 T cells that retained production of IFNγ, TNFα, perforin, and granzyme B. Combining acarbose with either anti-PD-1 or the mammalian target of rapamycin inhibitor, rapamycin, significantly reduced lung metastases relative to control mice on the same therapies. Our findings in mice suggest that combining acarbose with current RCC therapeutics may improve outcomes, warranting further study to determine whether acarbose can achieve similar responses in advanced RCC patients in a safe and likely cost-effective manner.

Indexed as

glucoseimmunityimmunotherapykidney cancernutrition

Identifiers

PMID33036247
PMCPMC7601245
OpenAlexW3091920370

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.