Evidence map›Paper›PMID 27382252›Full record

ArticleDrug design, development and therapy2016

MART-10, a newly synthesized vitamin D analog, represses metastatic potential of head and neck squamous carcinoma cells.

Shih-Wei Yang, Chi-Ying Tsai, Yi-Chun Pan, Chun-Nan Yeh, Jong-Hwei S Pang, Masashi Takano, Atsushi Kittaka, Horng-Heng Juang, Tai C Chen, Kun-Chun Chiang

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2016. 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
0.8field-weighted citation impact, top 24% 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, 16 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. The role of vitamin D in head and neck cancer.Laryngoscope investigative otolaryngology · 2020
    Review
  7. Impact of dietary vitamin D on initiation and progression of oral cancer.The Journal of steroid biochemistry and molecular biology · 2020
    Article
  8. 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

10 authors at 2 institutions in 2 countries.

Shih-Wei YangDepartment of Otolaryngology - Head and Neck Surgery, Chang Gung Memorial Hospital, Keelung, Taiwan, Republic of China.
Chi-Ying TsaiDepartment of Oral and Maxillofacial Surgery, Chang Gung Memorial Hospital, Taoyuan, Taiwan, Republic of China.
Yi-Chun PanDepartment of General Dentistry, Chang Gung Memorial Hospital, Chang Gung University, Keelung, Taiwan, Republic of China.
Chun-Nan YehGeneral Surgery Department, Chang Gung Memorial Hospital, Keelung, Taiwan, Republic of China.
Jong-Hwei S PangGraduate Institute of Clinical Medical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan, Republic of China.
Masashi TakanoFaculty of Pharmaceutical Sciences, Teikyo University, Tokyo, Japan.
Atsushi KittakaFaculty of Pharmaceutical Sciences, Teikyo University, Tokyo, Japan.
Horng-Heng JuangDepartment of Anatomy, College of Medicine, Chang Gung University, Taoyuan, Taiwan, Republic of China.
Tai C ChenEndocrine Core Laboratory, Boston University School of Medicine, Boston, MA, USA.
Kun-Chun ChiangGeneral Surgery Department, Chang Gung Memorial Hospital, Keelung, Taiwan, Republic of China; Zebrafish Center, Chang Gung Memorial Hospital, Keelung, Taiwan, Republic of China.
Chang Gung University · TWTeikyo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Even with multidisciplinary treatment, the prognosis and quality of life of patients diagnosed with head and neck squamous cell carcinoma (HNSCC) are still not satisfactory. Previously, 19-Nor-2α-(3-hydroxypropyl)-1α,25(OH)2D3 (MART-10), the new brand 1α,25(OH)2D3 analog, has been demonstrated to be an effective drug to inhibit HNSCC growth in vitro. Since most cancer patients die of metastasis, in this study, the antimetastatic effect of MART-10 on HNSCC was investigated. Our results reveal that both 1α,25(OH)2D3 and MART-10 effectively repressed the migration and invasion of HNSCC cells, with MART-10 being much more potent than 1α,25(OH)2D3. The antimetastatic effect of 1α,25(OH)2D3 and MART-10 was mediated by attenuation of epithelial-mesenchymal transition (EMT), which was supported by the finding that the expression of EMT-inducing transcriptional factors, Sail and Twist, was inhibited by 1α,25(OH)2D3 and MART-10. The upregulation of E-cadherin and downregulation of N-cadherin in FaDu cells induced by both drugs further confirmed the repression of EMT. In addition, 1α,25(OH)2D3 and MART-10 treatment inhibited intracellular MMP-9 expression and extracellular MMP activity in FaDu cells. Collectively, our results suggest that the less-calcemia 1α,25(OH)2D3 analog, MART-10, is a promising drug for HNSCC treatment. Further clinical studies are warranted.

Indexed as

Antineoplastic AgentsCarcinoma, Squamous CellCell Line, TumorCholecalciferolDown-RegulationEpithelial-Mesenchymal TransitionHead and Neck NeoplasmsHumansMatrix Metalloproteinase 9Neoplasm MetastasisVitamin D19-nor-2-(3-hydroxypropyl)-1,25-dihydroxyvitamin D3Antineoplastic AgentsCholecalciferolMatrix Metalloproteinase 9MMP9 protein, humanVitamin DEMThead and neck cancerMART-10metastasisvitamin D analog

Identifiers

PMID27382252
PMCPMC4918737
OpenAlexW2427168003

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.