Evidence map›Paper›PMID 33879557›Full record

ArticleMolecular cancer therapeutics2021

Sulindac Modulates the Response of Proficient MMR Colorectal Cancer to Anti-PD-L1 Immunotherapy.

Bin Yi, Hao Cheng, Dorota Wyczechowska, Qingzhao Yu, Li Li, Augusto C Ochoa, Adam I Riker, Yaguang Xi

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. 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

8 authors at 3 institutions in 1 country.

Bin YiDepartment of Genetics, School of Medicine, Louisiana State University Health Sciences Center, New Orleans, Louisiana.
Hao ChengDepartment of Genetics, School of Medicine, Louisiana State University Health Sciences Center, New Orleans, Louisiana.
Dorota WyczechowskaStanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, Louisiana.
Qingzhao YuSchool of Public Health, Louisiana State University Health Sciences Center, New Orleans, Louisiana.
Li LiOchsner Clinical School, University of Queensland, and Institute for Translational Research, Ochsner Clinic Foundation, New Orleans, Louisiana.
Augusto C OchoaStanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, Louisiana.
Adam I RikerGeaton and JoAnn DeCesaris Cancer Institute, Anne Arundel Medical Center, Luminis Health, Annapolis, Maryland.
Yaguang XiDepartment of Genetics, School of Medicine, Louisiana State University Health Sciences Center, New Orleans, Louisiana. yxi@lsuhsc.edu.ORCID 0000-0003-3681-9352
Louisiana State University Health Sciences Center New Orleans · USAnne Arundel Medical Center · USOchsner Medical Center · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI AUGUSTO C. OCHOA · 2012 to 2026
$69.1M
Understanding and Addressing Cancer Health Disparities in LouisianaP20CA233374 · NCI · LSU HEALTH SCIENCES CENTER · PI MIELE, LUCIO · 2018 to 2020
$2.9M
MicroRNA and colorectal cancer chemopreventionR01CA192395 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI XI, YAGUANG · 2015 to 2019
$1.9M
NCI NIH HHS P20 CA233374NCI NIH HHS R01 CA192395NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

Immune-checkpoint inhibitor (ICI) therapy has been widely used to treat different human cancers, particularly advanced solid tumors. However, clinical studies have reported that ICI immunotherapy benefits only ∼15% of patients with colorectal cancer, specifically those with tumors characterized by microsatellite instability (MSI), a molecular marker of defective DNA mismatch repair (dMMR). For the majority of patients with colorectal cancer who carry proficient MMR (pMMR), ICIs have shown little clinical benefit. In this study, we examined the efficacy of sulindac to enhance the response of pMMR colorectal cancer to anti-PD-L1 immunotherapy. We utilized a CT26 syngeneic mouse tumor model to compare the inhibitory effects of PD-L1 antibody (Ab), sulindac, and their combination on pMMR colorectal cancer tumor growth. We found that mice treated with combination therapy showed a significant reduction in tumor volume, along with increased infiltration of CD8

Indexed as

AnimalsAntineoplastic AgentsAntineoplastic Agents, ImmunologicalB7-H1 AntigenCell Line, TumorColorectal NeoplasmsDisease Models, AnimalDNA Mismatch RepairHumansImmune Checkpoint InhibitorsLymphocytes, Tumor-InfiltratingMiceNF-kappa BSignal TransductionSulindacTumor BurdenAntineoplastic AgentsAntineoplastic Agents, ImmunologicalB7-H1 AntigenCD274 protein, humanImmune Checkpoint InhibitorsNF-kappa BSulindac

Identifiers

PMID33879557
PMCPMC8295201
OpenAlexW3156698908

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.