Evidence map›Paper›PMID 32285621›Full record

ArticleJournal of cellular and molecular medicine2020

Calcitriol enhances Doxorubicin-induced apoptosis in papillary thyroid carcinoma cells via regulating VDR/PTPN2/p-STAT3 pathway.

Ting Zhang, Liang He, Zhihong Wang, Wenwu Dong, Wei Sun, Yuan Qin, Ping Zhang, Hao Zhang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Vitamin D-Related Genes and Thyroid Cancer-A Systematic Review.International journal of molecular sciences · 2022
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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

8 authors at 1 institution in 1 country.

Ting ZhangDepartment of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, China.
Liang HeDepartment of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, China.
Zhihong WangDepartment of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, China.
Wenwu DongDepartment of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, China.
Wei SunDepartment of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, China.
Yuan QinDepartment of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, China.
Ping ZhangDepartment of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, China.
Hao ZhangDepartment of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, China.ORCID 0000-0002-9938-8433
First Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is increasing evidence that vitamin D deficiency is the risk factor for multiple diseases, such as immune disorder, cardiovascular disease and cancer. Calcitriol is the active form of vitamin D with beneficial effects on anti-cancer by binding vitamin D receptor (VDR). The primary aim of this study was to investigate the role of Calcitriol on papillary thyroid carcinoma (PTC) and explore the possible mechanism. We found nuclear VDR expression in PTC samples was negatively correlated with STAT3 hyperphosphorylation that indicated worse PTC clinicopathologic characteristics. Calcitriol treatment up-regulated VDR and protein tyrosine phosphatase N 2 (PTPN2) expression, down-regulated signal transducers and activators of transcription (STAT3) phosphorylation and thereby facilitating chemotherapy drug Doxorubicin-induced apoptosis in PTC cell lines. However, the apoptosis-promoting effect of Calcitriol and Doxorubicin co-treatment was abrogated by STAT3 hyperphosphorylation, indicating suppression of STAT3 phosphorylation was essential for combined treatment of Calcitriol and Doxorubicin in PTC. Together, these results suggested that Calcitriol reinforced the sensitivity of PTC cells to Doxorubicin by regulating VDR/PTPN2/p-STAT3 signalling pathway.

Indexed as

AdultAgedApoptosisCalcitriolCell Line, TumorDoxorubicinFemaleHumansImmunohistochemistryMaleMiddle AgedNeoplasm MetastasisNeoplasm StagingPhosphorylationProtein Tyrosine Phosphatase, Non-Receptor Type 2Receptors, CalcitriolCalcitriolDoxorubicinProtein Tyrosine Phosphatase, Non-Receptor Type 2PTPN2 protein, humanReceptors, CalcitriolSTAT3 protein, humanSTAT3 Transcription FactorVDR protein, humanapoptosisCalcitriolpapillary thyroid carcinomavitamin D receptor

Identifiers

PMID32285621
PMCPMC7214146
OpenAlexW3015457994

What OpenQuestion holds

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LicenceCC BY
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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.