Evidence map›Paper›PMID 33510997›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2021

The Beneficial Role of Sunitinib in Tumor Immune Surveillance by Regulating Tumor PD-L1.

Hui Li, Xinwei Kuang, Long Liang, Youqiong Ye, YongChang Zhang, Jialu Li, Fangyu Ma, Juan Tao, Guang Lei, Shuang Zhao and 9 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.2field-weighted citation impact, top 6% 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

39 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
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  3. Review
  4. Article
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  6. Article
  7. Review
  8. Zosuquidar Promotes Antitumor Immunity by Inducing Autophagic Degradation of PD-L1.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. The evolving landscape of PCSK9 inhibition in cancer.European journal of pharmacology · 2023
    Review
  19. Article
  20. Review
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

19 authors at 7 institutions in 4 countries.

Hui LiDepartment of Dermatology Xiangya Hospital Central South University Changsha Hunan 410008 China.ORCID https://orcid.org/0000-0003-1086-0402
Xinwei KuangDepartment of Dermatology Xiangya Hospital Central South University Changsha Hunan 410008 China.
Long LiangDepartment of Dermatology Xiangya Hospital Central South University Changsha Hunan 410008 China.
Youqiong YeShanghai Institute of Immunology Department of Immunology and Microbiology Center for Single-Cell Omics State Key Laboratory of Oncogenes and Related Genes Shanghai Jiao Tong University School of Medicine Shanghai 200025 China.
YongChang ZhangDepartment of Medical Oncology Lung Cancer and Gastrointestinal Unit Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine Central South University Changsha Hunan 410013 China.
Jialu LiDepartment of Biostatistics HuaJia Biomedical Intelligence ShenZhen 518054 China.
Fangyu MaDepartment of Health Management Center Xiangya Hospital Central South University Changsha Hunan 410008 China.
Juan TaoDepartment of Dermatology Affiliated Union Hospital Tongji Medical College Huazhong University of Science and Technology Wuhan 430022 China.
Guang LeiDepartment of Radiation Oncology Hunan Cancer Hospital and The Affiliated Cancer Hospital of Xiangya School of Medicine Central South University Changsha Hunan 410013 China.
Shuang ZhaoDepartment of Dermatology Xiangya Hospital Central South University Changsha Hunan 410008 China.
Juan SuDepartment of Dermatology Xiangya Hospital Central South University Changsha Hunan 410008 China.
Nong YangDepartment of Medical Oncology Lung Cancer and Gastrointestinal Unit Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine Central South University Changsha Hunan 410013 China.
Cong PengDepartment of Dermatology Xiangya Hospital Central South University Changsha Hunan 410008 China.
Xiaowei XuDepartment of Pathology and Laboratory Medicine Perelman School of Medicine 42 University of Pennsylvania Philadelphia PA 19104 USA.
Mien-Chie HungGraduate Institute of Biomedical Sciences and Center for Molecular Medicine China 44 Medical University Taichung 404 Taiwan.
Leng HanDepartment of Biochemistry and Molecular Biology The University of Texas Health Science Center at Houston McGovern Medical School Houston TX 77030 USA.
Hong LiuDepartment of Dermatology Xiangya Hospital Central South University Changsha Hunan 410008 China.
Jing LiuMolecular Biology Research Center Center for Medical Genetics Hunan Province Key Laboratory of Basic and Applied Hematology School of Life Sciences Central South University Changsha 410078 China.
Xiang ChenDepartment of Dermatology Xiangya Hospital Central South University Changsha Hunan 410008 China.
Central South University · CNAsia University · TWBeijing Huajia University · CNShanghai Jiao Tong University · CNThe University of Texas Health Science Center · USUnion Hospital · CNUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoints blockades have shown promising clinical effects in various malignancies, but the overall response rate is low. Here, the immune features are comprehensively characterized in >10 000 cancer patients from The Cancer Genome Atlas and significantly positive correlations are observed between targets of Sunitinib and inhibitory immune checkpoints and suppressive immune cells. It is further confirmed that Sunitinib treatment increases the antitumor immunity in a phase III trial. Mechanistically, it is discovered that Sunitinib regulates the stability of tumor PD-L1 via p62, that p62 can bind to PD-L1 and specifically promote its translocation into autophagic lysosome for degradation. Preclinically, Sunitinib shows a synergistic antitumor effect with cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) monoclonal antibody (mAb) in melanoma and nonsmall cell lung cancer (NSCLC) immune competent mice by promoting the tumor-infiltrating lymphocytes activity. Clinically, a higher PD-L1 level but a lower p62 level in the tumor region of responders as compared to those of nonresponders among anti-PD-1-treated NSCLC patients is observed. Taken together, by utilizing rigorous computational analysis, functional characterization in vitro and in vivo, and neoadjuvent clinical trial, a novel molecular mechanism is revealed regarding the regulation of PD-L1 via p62, thus providing a novel therapeutic strategy by the combination treatment of CTLA-4 with Sunitinib.

Indexed as

immune surveillancep62PD‐L1selective autophagysunitinib

Identifiers

PMID33510997
PMCPMC7816704
OpenAlexW3110058912

What OpenQuestion holds

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Registered trials

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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.