Evidence map›Paper›PMID 35440620›Full record

ArticleNature communications2022

Targeting TCTP sensitizes tumor to T cell-mediated therapy by reversing immune-refractory phenotypes.

Hyo-Jung Lee, Kwon-Ho Song, Se Jin Oh, Suyeon Kim, Eunho Cho, Jungwon Kim, Yun Gyu Park, Kyung-Mi Lee, Cassian Yee, Seung-Hwa Song and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 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
1.7field-weighted citation impact, top 14% 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, 17 citations in OpenAlex.

  1. Review
  2. Article
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  4. Overcoming resistance to anti-PD-1/PD-L1 therapy in cancer.Cancer drug resistance (Alhambra, Calif.) · 2026
    Review
  5. Article
  6. Article
  7. Review
  8. Article
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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

14 authors at 4 institutions in 4 countries.

Hyo-Jung LeeDepartment of Biochemistry and Molecular Biology, Korea university College of Medicine, Seoul, 02841, Republic of Korea.
Kwon-Ho SongResearch Institute of Biomedical Engineering and Department of Medicine, Catholic University of Daegu School of Medicine, Daegu, Republic of Korea.
Se Jin OhDepartment of Biochemistry and Molecular Biology, Korea university College of Medicine, Seoul, 02841, Republic of Korea.
Suyeon KimDepartment of Biochemistry and Molecular Biology, Korea university College of Medicine, Seoul, 02841, Republic of Korea.ORCID http://orcid.org/0000-0002-3691-7692
Eunho ChoDepartment of Biochemistry and Molecular Biology, Korea university College of Medicine, Seoul, 02841, Republic of Korea.
Jungwon KimDepartment of Biochemistry and Molecular Biology, Korea university College of Medicine, Seoul, 02841, Republic of Korea.
Yun Gyu ParkDepartment of Biochemistry and Molecular Biology, Korea university College of Medicine, Seoul, 02841, Republic of Korea.
Kyung-Mi LeeDepartment of Biochemistry and Molecular Biology, Korea university College of Medicine, Seoul, 02841, Republic of Korea.ORCID http://orcid.org/0000-0002-5378-9258
Cassian YeeDepartment of Melanoma Medical Oncology and Immunology, U.T. MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0002-4429-7307
Seung-Hwa SongDepartment of Biochemistry and Molecular Biology, Korea university College of Medicine, Seoul, 02841, Republic of Korea.ORCID http://orcid.org/0000-0002-0015-4435
Suhwan ChangDepartment of Biomedical Sciences, University of Ulsan College of Medicine, Asan Medical Center, Seoul, 05505, Republic of Korea.ORCID http://orcid.org/0000-0002-0282-0120
Jungmin ChoiDepartment of Biomedical Science, Korea university College of Medicine, Seoul, 02841, Republic of Korea.ORCID http://orcid.org/0000-0002-8614-0973
Sang Taek JungDepartment of Biomedical Science, Korea university College of Medicine, Seoul, 02841, Republic of Korea.ORCID http://orcid.org/0000-0001-7217-979X
Tae Woo KimDepartment of Biochemistry and Molecular Biology, Korea university College of Medicine, Seoul, 02841, Republic of Korea. twkim0421@korea.ac.kr.
Korea University · KRDaegu Catholic University · KRThe University of Texas MD Anderson Cancer Center · USUlsan College · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy has emerged as a powerful approach to cancer treatment. However, immunotherapeutic resistance limits its clinical application. Therefore, identifying immune-resistant factors, which can be targeted by clinically available drugs and it also can be a companion diagnostic marker, is needed to develop combination strategies. Here, using the transcriptome data of patients, and immune-refractory tumor models, we identify TCTP as an immune-resistance factor that correlates with clinical outcome of anti-PD-L1 therapy and confers immune-refractory phenotypes, decreased T cell trafficking to the tumor and resistance to cytotoxic T lymphocyte-mediated tumor cell killing. Mechanistically, TCTP activates the EGFR-AKT-MCL-1/CXCL10 pathway by phosphorylation-dependent interaction with Na, K ATPase. Furthermore, treatment with dihydroartenimsinin, the most effective agent impending the TCTP-mediated-refractoriness, synergizes with T cell-mediated therapy to control immune-refractory tumors. Thus, our findings suggest a role of TCTP in promoting immune-refractoriness, thereby encouraging a rationale for combination therapies to enhance the efficacy of T cell-mediated therapy.

Indexed as

B7-H1 AntigenImmunotherapyCell Line, TumorCombined Modality TherapyHumansPhenotypeTumor MicroenvironmentB7-H1 Antigen

Identifiers

PMID35440620
PMCPMC9019109
OpenAlexW4226120074

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.