Evidence map›Paper›PMID 37014700›Full record

ArticleThe Journal of clinical investigation2023

Long noncoding RNA HITT coordinates with RGS2 to inhibit PD-L1 translation in T cell immunity.

Qingyu Lin, Tong Liu, Xingwen Wang, Guixue Hou, Zhiyuan Xiang, Wenxin Zhang, Shanliang Zheng, Dong Zhao, Qibin Leng, Xiaoshi Zhang and 4 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2023. 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
6.7field-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

17 citing papers in PubMed, 28 citations in OpenAlex.

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  5. G protein regulation by RGS proteins in the pathophysiology of dilated cardiomyopathy.American journal of physiology. Heart and circulatory physiology · 2025
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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 5 institutions in 1 country.

Qingyu LinSchool of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Tong LiuDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Heilongjiang Academy of Medical Sciences, Harbin, China.
Xingwen WangSchool of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Guixue HouBGI-SHENZHEN, Shenzhen, China.
Zhiyuan XiangSchool of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Wenxin ZhangSchool of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Shanliang ZhengSchool of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Dong ZhaoSchool of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Qibin LengAffiliated Cancer Hospital and Institute of Guangzhou Medical University, State Key Laboratory of Respiratory Disease, Guangzhou, China.
Xiaoshi ZhangDepartment of Clinical Laboratory, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Minqiao LuSchool of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Tianqi GuanSchool of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Hao LiuSchool of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Ying HuSchool of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Harbin Institute of Technology · CNBGI Group (China) · CNHarbin Medical University · CNQilu Hospital of Shandong University · CNState Key Laboratory of Respiratory Disease · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmed cell death ligand 1 (PD-L1) is an immune checkpoint protein frequently expressed in human cancers that contributes to immune evasion through its binding to PD-1 on activated T cells. Unveiling the mechanisms underlying PD-L1 expression is essential for understanding the impact of the immunosuppressive microenvironment and is also crucial for the purpose of reboosting antitumor immunity. However, how PD-L1 is regulated, particularly at translational levels, remains largely unknown. Here, we discovered that a long noncoding RNA (lncRNA), HIF-1α inhibitor at translation level (HITT), was transactivated by E2F transcription factor 1 (E2F1) under IFN-γ stimulation. It coordinated with regulator of G protein signaling 2 (RGS2) in binding to the 5' UTR of PD-L1, resulting in reduced PD-L1 translation. HITT expression enhanced T cell-mediated cytotoxicity both in vitro and in vivo in a PD-L1-dependent manner. The clinical correlation between HITT/PD-L1 and RGS2/PD-L1 expression was also detected in breast cancer tissues. Together, these findings demonstrate the role of HITT in antitumor T cell immunity, highlighting activation of HITT as a potential therapeutic strategy for enhancing cancer immunotherapy.

Indexed as

Breast NeoplasmsRGS ProteinsRNA, Long NoncodingB7-H1 AntigenCell Line, TumorFemaleHumansImmunotherapyT-LymphocytesTumor MicroenvironmentB7-H1 AntigenRGS2 protein, humanRGS ProteinsRNA, Long NoncodingCancer immunotherapyImmunologyOncology

Identifiers

PMID37014700
PMCPMC10231998
OpenAlexW4362523759

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.