Evidence map›Paper›PMID 29361818›Full record

ArticleCancer research and treatment2018

Preclinical Study of Novel Curcumin Analogue SSC-5 Using Orthotopic Tumor Xenograft Model for Esophageal Squamous Cell Carcinoma.

Lai Nar Tung, Senchuan Song, Kin Tak Chan, Mei Yuk Choi, Ho Yu Lam, Chung Man Chan, Zhiyong Chen, Hector K Wang, Hoi Ting Leung, Simon Law and 3 more

Open access · diamondAbstract read
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Article in Cancer research and treatment, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 37% 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

7 citing papers in PubMed, 15 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 4 institutions in 2 countries.

Lai Nar TungDepartment of Surgery, The University of Hong Kong, Hong Kong.
Senchuan SongSchool of Chemical Engineering and Technology, Sun Yat-Sen University, Guangzhou, China.
Kin Tak ChanDepartment of Surgery, The University of Hong Kong, Hong Kong.
Mei Yuk ChoiDepartment of Surgery, The University of Hong Kong, Hong Kong.
Ho Yu LamDepartment of Surgery, The University of Hong Kong, Hong Kong.
Chung Man ChanDepartment of Surgery, The University of Hong Kong, Hong Kong.
Zhiyong ChenGuangdong Petrochemical Research Institute, Guangzhou, China.
Hector K WangDepartment of Surgery, The University of Hong Kong, Hong Kong.
Hoi Ting LeungDepartment of Surgery, The University of Hong Kong, Hong Kong.
Simon LawDepartment of Surgery, The University of Hong Kong, Hong Kong.
Yanmin HuangGuangxi Teachers Education University, College of Chemistry and Materials Science, Nanning, China.
Huacan SongSchool of Chemical Engineering and Technology, Sun Yat-Sen University, Guangzhou, China.
Nikki P LeeDepartment of Surgery, The University of Hong Kong, Hong Kong.
University of Hong Kong · HKSun Yat-sen University · CNZhejiang University · CNGuangdong University of Petrochemical Technology · CN

Funding

Research Grants Council T42-103/16-N
6 · The paper itself

Abstract

purposeTumor xenograft model is an indispensable animal cancer model. In esophageal squamous cell carcinoma (ESCC) research, orthotopic tumor xenograft model establishes tumor xenograft in the animal esophagus, which allows the study of tumorigenesis in its native microenvironment. MATERIALS AND

methodsIn this study,we described two simple and reproducible methods to develop tumor xenograft at the cervical or the abdominal esophagus in nude mice by direct injection of ESCC cells in the esophageal wall.

resultsIn comparing these two methods, the cervical one presented with more clinically relevant features, i.e., esophageal stricture, body weight loss and poor survival. In addition, the derived tumor xenografts accompanied a rapid growth rate and a high tendency to invade into the surrounding structures. This model was subsequently used to study the anti-tumor effect of curcumin, which is known for its potential therapeutic effects in various diseases including cancers, and its analogue SSC-5. SSC-5 was selected among the eight newly synthesized curcumin analogues based on its superior anti-tumor effect demonstrated in an MTT cell proliferation assay and its effects on apoptosis induction and cell cycle arrest in cultured ESCC cells. Treatment of orthotopic tumor-bearing mice with SSC-5 resulted in an inhibition in tumor growth and invasion.

conclusionTaken together, we have established a clinically relevant orthotopic tumor xenograft model that can serve as a preclinical tool for screening new anti-tumor compounds, e.g., SSC-5, in ESCC.

Indexed as

AbdomenAnimalsCatecholsCell Line, TumorCell ProliferationCell SurvivalCervix UteriCurcuminDrug Screening Assays, AntitumorEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaFemaleHumansMiceMice, NudeNeoplasm TransplantationCatecholsCurcuminCurcuminEsophageal squamous cell carcinoma

Identifiers

PMID29361818
PMCPMC6192909
OpenAlexW2785022704

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.