Evidence map›Paper›PMID 31802389›Full record

ArticleHepatology international2020

Targeting adenosinergic pathway enhances the anti-tumor efficacy of sorafenib in hepatocellular carcinoma.

Jing Liao, Dan-Ni Zeng, Jin-Zhu Li, Qiao-Min Hua, Zhiyu Xiao, Chuanchao He, Kai Mao, Ling-Yan Zhu, Yifan Chu, Wei-Ping Wen and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Hepatology international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Heliyon · 2024
    Article
  7. Review
  8. Article
  9. The Immune Regulatory Role of Adenosine in the Tumor Microenvironment.International journal of molecular sciences · 2023
    Review
  10. Article
  11. Tumor-associated myeloid cells in cancer immunotherapy.Journal of hematology & oncology · 2023
    Review
  12. Review
  13. Review
  14. Article
  15. Type I IFNs repolarized a CD169Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
  16. High S100A9Aging · 2021
    Article
  17. 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

12 authors at 1 institution in 1 country.

Jing LiaoMOE Key Laboratory of Gene Function and Regulation, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, Guangdong, China.
Dan-Ni ZengMOE Key Laboratory of Gene Function and Regulation, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, Guangdong, China.
Jin-Zhu LiMOE Key Laboratory of Gene Function and Regulation, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, Guangdong, China.
Qiao-Min HuaMOE Key Laboratory of Gene Function and Regulation, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, Guangdong, China.
Zhiyu XiaoDepartment of Hepatobiliary Surgery, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Guangzhou, 510289, Guangdong, China.
Chuanchao HeDepartment of Hepatobiliary Surgery, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Guangzhou, 510289, Guangdong, China.
Kai MaoDepartment of Hepatobiliary Surgery, Sun Yat-Sen Memorial Hospital, Sun Yat-sen University, Guangzhou, 510289, Guangdong, China.
Ling-Yan ZhuMOE Key Laboratory of Gene Function and Regulation, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, Guangdong, China.
Yifan ChuMOE Key Laboratory of Gene Function and Regulation, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, Guangdong, China.
Wei-Ping WenGuangdong Institute of Gastroenterology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510655, Guangdong, China.
Limin ZhengMOE Key Laboratory of Gene Function and Regulation, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, Guangdong, China.
Yan WuMOE Key Laboratory of Gene Function and Regulation, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, Guangdong, China. wuyan32@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0001-6613-2696
Sun Yat-sen University · CN

Funding

China Postdoctoral Science Foundation 2018M643302Fundamental Research Funds for the Central Universities 171gjc32National Key Research and Development Plan of China 2018ZX10302205National Natural Science Foundation of China 31900651National Natural Science Foundation of China 81773054
6 · The paper itself

Abstract

backgroundSorafenib is the most widely used first-line treatment for patients with advanced hepatocellular carcinoma (HCC), but such treatment provides only limited survival benefits that might be related to the immune status of distinct tumor microenvironments. A fundamental understanding of the distribution and phenotypes of T lymphocytes in tumors will undoubtedly lead to the development of novel immunotherapeutic strategies that could possibly enhance the efficacy of sorafenib treatments.

methodsFlow cytometry, immunohistochemistry and immunofluorescence analyses were performed to detect the infiltration and distribution of various leukocyte populations, and the expression of different immune checkpoint molecules in fresh HCC tumor tissues. Correlations among indicating genes were calculated in 365 patients with HCC from The Cancer Genome Atlas (TCGA) data set, and the cumulative overall survival time was calculated using the Kaplan-Meier method. Moreover, role of adenosinergic pathway on sorafenib anti-tumor efficacy was investigated using both subcutaneous and orthotopic transplantation tumor model in immune competent C57BL/6 mice.

resultsWe revealed that levels of CD3

conclusionsThese results suggest that adenosinergic pathway might represent an applicable target for sorafenib-combined-therapies in human HCC.

Indexed as

AdolescentAdultAgedAged, 80 and overAnimalsAntineoplastic AgentsCarcinoma, HepatocellularCell Line, TumorDisease Models, AnimalFemaleHumansLiver NeoplasmsMaleMiceMice, Inbred C57BLMiddle AgedAntineoplastic AgentsSorafenibAdenosinergic pathwayHepatocellular carcinomaImmunotherapySorafenibT cells exhaustion

Identifiers

PMID31802389
OpenAlexW2992820774

What OpenQuestion holds

Textmetadata
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.