Evidence map›Paper›PMID 33824475›Full record

ArticleOncogene2021

Protein tyrosine phosphatase receptor type D gene promotes radiosensitivity via STAT3 dephosphorylation in nasopharyngeal carcinoma.

Yanling Lin, Xiaohan Zhou, Kaifan Yang, Yuting Chen, Lingzhi Wang, Wenxiao Luo, Yujiang Li, Jinrong Liao, Yingtong Zhou, Yiming Lei and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

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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

13 authors at 3 institutions in 1 country.

Yanling Lin *Department of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID http://orcid.org/0000-0003-3215-0890
Xiaohan Zhou *Department of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Kaifan Yang *Division of Spine Surgery, Department of Orthopaedics, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID http://orcid.org/0000-0003-4166-0198
Yuting ChenDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Lingzhi WangFirst Clinical Medical College, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Wenxiao LuoDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yujiang LiDepartment of Thoracic and Cardiovascular Surgery/Huiqiao Medical Center, Southern Medical University, Guangzhou, China.
Jinrong LiaoSecond Clinical Medical College, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Yingtong ZhouDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yiming LeiFirst Clinical Medical College, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yanting ZhangFirst Clinical Medical College, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Dehua WuDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China. wudehua.gd@gmail.com.ORCID http://orcid.org/0000-0003-0560-0016
Longmei CaiDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China. cailongmeibestlove@163.com.ORCID http://orcid.org/0000-0003-0421-464X
Nanfang Hospital · CNDongguan People’s Hospital · CNZhujiang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Radiotherapy is essential to the treatment of nasopharyngeal carcinoma (NPC) and acquired or innate resistance to this therapeutic modality is a major clinical problem. However, the underlying molecular mechanisms in the radiation resistance in NPC are not fully understood. Here, we reanalyzed the microarray data from public databases and identified the protein tyrosine phosphatase receptor type D (PTPRD) as a candidate gene. We found that PTPRD was downregulated in clinical NPC tissues and NPC cell lines with its promoter hypermethylated. Functional assays revealed that PTPRD overexpression sensitized NPC to radiation in vitro and in vivo. Importantly, miR-454-3p directly targets PTPRD to inhibit its expression and biological effect. Interestingly, mechanistic analyses indicate that PTPRD directly dephosphorylates STAT3 to enhance Autophagy-Related 5 (ATG5) transcription, resulting in triggering radiation-induced autophagy. The immunohistochemical staining of 107 NPC revealed that low PTPRD and high p-STAT3 levels predicted poor clinical outcome. Overall, we showed that PTPRD promotes radiosensitivity by triggering radiation-induced autophagy via the dephosphorylation of STAT3, thus providing a potentially useful predictive biomarker for NPC radiosensitivity and drug target for NPC radiosensitization.

Indexed as

Nasopharyngeal CarcinomaNasopharyngeal NeoplasmsRadiation ToleranceReceptor-Like Protein Tyrosine Phosphatases, Class 2STAT3 Transcription FactorAnimalsAutophagyCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansMaleMiceMice, NudeMicroRNAsPhosphorylationMicroRNAsPTPRD protein, humanReceptor-Like Protein Tyrosine Phosphatases, Class 2STAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID33824475
PMCPMC8084736
OpenAlexW3148505793

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.