Evidence map›Paper›PMID 30537218›Full record

ArticleHead & neck2019

Anti-oral cancer effects of triptolide by downregulation of DcR3 in vitro, in vivo, and in preclinical patient-derived tumor xenograft model.

Cheng-Yu Yang, Chih-Kung Lin, Cheng-Chih Hsieh, Chang-Huei Tsao, Chun-Shu Lin, Bo Peng, Yen-Tzu Chen, Chun-Chieh Ting, Wei-Chin Chang, Gu-Jiun Lin and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Head & neck, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 21% 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, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Metronomic Therapy in Oral Squamous Cell Carcinoma.Journal of clinical medicine · 2021
    Review
  9. Article
  10. 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 3 institutions in 1 country.

Cheng-Yu YangSchool of Dentistry, National Defense Medical Center, Taipei, Taiwan.
Chih-Kung LinDivision of Anatomic Pathology, Taipei Tzu Chi Hospital, Taipei, Taiwan.
Cheng-Chih HsiehDepartment of Pharmacy Practice, Tri-Service General Hospital, Taipei, Taiwan.
Chang-Huei TsaoGraduate Institute of Microbiology and Immunology, National Defense Medical Center, Taipei, Taiwan.
Chun-Shu LinDepartment of Radiation Oncology, Tri-Service General Hospital, National Defense Medical Centre, Taipei, Taiwan.ORCID 0000-0003-1919-8769
Bo PengSchool of Dentistry, National Defense Medical Center, Taipei, Taiwan.
Yen-Tzu ChenSchool of Dentistry, National Defense Medical Center, Taipei, Taiwan.
Chun-Chieh TingSchool of Dentistry, National Defense Medical Center, Taipei, Taiwan.
Wei-Chin ChangSchool of Dentistry, National Defense Medical Center, Taipei, Taiwan.
Gu-Jiun LinDepartment of Biology and Anatomy, National Defense Medical Center, Taipei, Taiwan.
Huey-Kang SytwuGraduate Institute of Microbiology and Immunology, National Defense Medical Center, Taipei, Taiwan.
Yuan-Wu ChenSchool of Dentistry, National Defense Medical Center, Taipei, Taiwan.ORCID 0000-0003-1927-7088
Tri-Service General Hospital · TWNational Defense Medical Center · TWTaipei Tzu Chi Hospital · TW

Funding

Cardinal Tien Hospital, Taipei, Taiwan, Republic of China CJH107A-2C01Medical Affairs Bureau, Ministry of National Defense, Taiwan, Republic of China MAB-106-090Ministry of Science and Technology, Taiwan, Republic of China MOST 105-2314-B-016-021-MY3Tri-Service General Hospital, Taiwan, Republic of China TSGH-C105-006-008-S05, TSGH-C106-004-006-008-S05, TSGH-C107-008-S06
6 · The paper itself

Abstract

backgroundAberrant expression of decoy receptor 3 (DcR3) is considered to be a diagnostic and therapeutic target for human cancers. The aim of this study was to assess DcR3 as a target of the anticancer effects of triptolide (TPL) in preclinical patient-derived tumor xenograft (PDTX) models of oral squamous cell carcinoma (OSCC).

methodsThe expression of DcR3 was evaluated through immunohistochemistry, and correlations were examined using clinical variables. The effects of TPL on the expression of DcR3 and cell proliferation were investigated in OSCC cell lines and in PDTX models.

resultsDcR3 overexpression was associated with overall survival and tumor size. TPL significantly decreased tumor growth. Moreover, TPL inhibited the expression of metastasis-associated protein 1 (MTA1), a transcription factor for DcR3 in vivo, in vitro, and in PDTX models.

conclusionTPL appeared to exert anticancer effects by repressing DcR3 and MTA1 in vitro, in vivo, and in PDTX models.

Indexed as

AnimalsAntineoplastic Agents, AlkylatingBiomarkers, TumorCarcinoma, Squamous CellCell ProliferationDiterpenesDown-RegulationEpoxy CompoundsHeterograftsHumansImmunohistochemistryMiceMice, Inbred NODMouth NeoplasmsPhenanthrenesReceptors, Tumor Necrosis Factor, Member 6bAntineoplastic Agents, AlkylatingBiomarkers, TumorDiterpenesEpoxy CompoundsPhenanthrenesReceptors, Tumor Necrosis Factor, Member 6btriptolidedecoy receptor 3 (DcR3)metastasis-associated protein 1 (MTA1)oral squamous cell carcinoma (OSCC)patient-derived tumor xenograft (PDTX)triptolide

Identifiers

PMID30537218
PMCPMC6590365
OpenAlexW2904525971

What OpenQuestion holds

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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.