Evidence map›Paper›PMID 20304669›Full record

ReviewCritical reviews in oncology/hematology2011

Targeting immune suppressing myeloid-derived suppressor cells in oncology.

Johnny Kao, Eric C Ko, Samuel Eisenstein, Andrew G Sikora, Shibo Fu, Shu-Hsia Chen

Abstract readReview
In one paragraph

Review in Critical reviews in oncology/hematology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 145 citations in OpenAlex.

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  20. Interactions among myeloid regulatory cells in cancer.Cancer immunology, immunotherapy : CII · 2019
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13 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Johnny KaoDepartment of Radiation Oncology, Mount Sinai School of Medicine, New York, NY 10029, United States. johnny.rao@mountsinai.org
Eric C Ko
Samuel Eisenstein
Andrew G Sikora
Shibo Fu
Shu-Hsia Chen
Icahn School of Medicine at Mount Sinai · US

Funding

Intervention of immune tolerance by small molecules to enhance immune therapyR01CA127483 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHEN, SHU-HSIA · 2008 to 2018
$3.4M
Myeloid Suppressor Cell-Mediated Immune Suppression of Tumor Specific T CellsR01CA109322 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHEN, SHU-HSIA · 2006 to 2015
$3.2M
Combination gene therapy for metastatic colon cancerR01CA070337 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI CHEN, SHU-HSIA · 2002 to 2010
$2.7M
NCI NIH HHS R01 CA070337NCI NIH HHS R01 CA109322NCI NIH HHS R01 CA127483
6 · The paper itself

Abstract

Emerging data suggests that host immune cells with a suppressive phenotype represent a significant hurdle to successful therapy for metastatic cancer. Among the suppressor cells, T regulatory cells (Treg) and myeloid-derived suppressor cells (MDSC) are significantly increased in hosts with advanced malignancies. MDSC mediate the suppression of the tumor antigen-specific T cell response through the induction of T cell anergy and the development of Treg in tumor-bearing mice. These results provide robust evidence of an in vivo immunoregulatory function of MDSC in the establishment of tumor antigen-specific tolerance and the development of Treg in tumor-bearing hosts. To achieve effective anti-tumor immunity, tumor-induced immunosuppression must be reversed. Our preliminary results indicate that c-kit ligand (stem cell factor) expressed by tumor cells may be required for MDSC accumulation in tumor-bearing mice, and that blocking the c-kit ligand/c-kit receptor interaction can prevent the development of Treg and reverse immune tolerance induced by MDSC. Since c-kit can be readily inhibited by several small molecule inhibitors including imatinib, sunitinib and dasatinib, targeting immune suppressing cells can be readily accomplished in the clinic.

Indexed as

AnimalsAntineoplastic AgentsCD11b AntigenHumansImmune ToleranceImmunotherapyIndolesMyeloid CellsNeoplasmsNeovascularization, PathologicProto-Oncogene Proteins c-kitPyrrolesSunitinibTumor MicroenvironmentVascular Endothelial Growth Factor AAntineoplastic AgentsCD11b AntigenIndolesProto-Oncogene Proteins c-kitPyrrolesSunitinibVascular Endothelial Growth Factor A

Identifiers

PMID20304669
PMCPMC2927714
OpenAlexW2065942096

What OpenQuestion holds

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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.