Evidence map›Paper›PMID 35869130›Full record

ArticleScientific reports2022

Blockade of CD47 enhances the antitumor effect of macrophages in renal cell carcinoma through trogocytosis.

Ha-Ram Park, Seong-Eun Kim, Bhumsuk Keam, Hyewon Chung, Seung Hyeok Seok, Soyeon Kim, Miso Kim, Tae Min Kim, Junsang Doh, Dong-Wan Kim and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

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  12. Intercellular Transfer of Immune Regulatory Molecules Via Trogocytosis.Results and problems in cell differentiation · 2024
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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

11 authors at 3 institutions in 1 country.

Ha-Ram ParkSeoul National University Cancer Research Institute, Seoul, Republic of Korea.
Seong-Eun KimDepartment of Mechanical Engineering, Pohang University of Science and Technology, Pohang, Republic of Korea.
Bhumsuk KeamSeoul National University Cancer Research Institute, Seoul, Republic of Korea. bhumsuk@snu.ac.kr.
Hyewon ChungDepartment of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Seung Hyeok SeokDepartment of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Soyeon KimSeoul National University Cancer Research Institute, Seoul, Republic of Korea.
Miso KimSeoul National University Cancer Research Institute, Seoul, Republic of Korea.
Tae Min KimSeoul National University Cancer Research Institute, Seoul, Republic of Korea.
Junsang DohDepartment of Materials Science and Engineering, Seoul National University, Seoul, Republic of Korea.
Dong-Wan KimSeoul National University Cancer Research Institute, Seoul, Republic of Korea.
Dae Seog HeoDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Seoul National University · KRSeoul National University Hospital · KRPohang University of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitors and vascular endothelial growth factor receptor tyrosine kinase inhibitors (VEGFR TKIs) are mainstream treatments for renal cell carcinoma (RCC). Both T cells and macrophages infiltrate the tumor microenvironment of RCC. CD47, an immune checkpoint of macrophages, transmits the "don't eat me" signal to macrophages. We propose a novel therapeutic strategy that activates the antitumor effect of macrophages. We found that CD47 was expressed in patients with RCC, and high CD47 expression was indicative of worse overall survival in datasets from The Cancer Genome Atlas. We observed that CD47-blocking antibodies enhanced the antitumor effect of macrophages against human RCC cell lines. Trogocytosis, rather than phagocytosis, occurred and was promoted by increased cell-to-cell contact between macrophages and RCC cells. Trogocytosis induced by CD47 blockade occurred in the presence of CD11b integrin signaling in macrophages and was augmented when RCC cells were exposed to VEGFR TKIs, except for sunitinib. In conclusion, this study presents evidence that anti-CD47 blocking antibodies improve the antitumor effect of macrophages in RCC. In combination with VEGFR TKIs, CD47 blockade is a potential therapeutic strategy for patients with RCC.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsAntibodies, BlockingAntigens, DifferentiationCD47 AntigenHumansMacrophagesPhagocytosisReceptors, ImmunologicTrogocytosisTumor MicroenvironmentVascular Endothelial Growth Factor AAntibodies, BlockingAntigens, DifferentiationCD47 AntigenCD47 protein, humanReceptors, ImmunologicVascular Endothelial Growth Factor A

Identifiers

PMID35869130
PMCPMC9307775
OpenAlexW4286487968

What OpenQuestion holds

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LicenceCC BY
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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.