Evidence map›Paper›PMID 31663659›Full record

ArticleCell proliferation2020

Pre-clinical evidences for the efficacy of tryptanthrin as a potent suppressor of skin cancer.

Mohan Shankar G, Vijai V Alex, Amrutha Nisthul A, Smitha V Bava, Sankar Sundaram, Archana P Retnakumari, Sadasivan Chittalakkottu, Ruby John Anto

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

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  13. Engineering diabetic human skin equivalent forFrontiers in bioengineering and biotechnology · 2022
    Article
  14. Article
  15. Experimental research in topical psoriasis therapy (Review).Experimental and therapeutic medicine · 2021
    Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Plants (Basel, Switzerland) · 2020
    Review
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 5 institutions in 1 country.

Mohan Shankar GDivision of Cancer Research, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram, Kerala, India.
Vijai V AlexDivision of Cancer Research, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram, Kerala, India.
Amrutha Nisthul ADepartment of Biotechnology and Microbiology, Kannur University, Kannur, Kerala, India.
Smitha V BavaDepartment of Biotechnology, University of Calicut, Calicut, Kerala, India.
Sankar SundaramDepartment of Pathology, Government Medical College, Kottayam, Kerala, India.
Archana P RetnakumariDivision of Cancer Research, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram, Kerala, India.
Sadasivan ChittalakkottuDepartment of Biotechnology and Microbiology, Kannur University, Kannur, Kerala, India.
Ruby John AntoDivision of Cancer Research, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram, Kerala, India.ORCID https://orcid.org/0000-0001-5856-0076
Rajiv Gandhi Centre for Biotechnology · INKannur University · INGovernment Medical College · INManipal Academy of Higher Education · INUniversity of Calicut · IN

Funding

Department of Biotechnology , Ministry of Science and TechnologyIndian Council of Medical Research no.3/1/3/JRF-2013/HRD-085Indian Council of Medical Research no.59/36/2013/online/BMS/TRM
6 · The paper itself

Abstract

objectiveClinical trials have demonstrated the efficacy of indigo naturalis, a traditional Chinese medicine ingredient, against psoriasis, a skin disease characterized by keratinocyte hyperproliferation and inflammation. The present study investigates the efficacy of tryptanthrin, a bioactive compound in indigo naturalis, against non-melanoma skin cancer (NMSC) and the signalling events involved.

methodsEfficacy of tryptanthrin against NMSC was assessed using DMBA/PMA-induced skin carcinogenesis model in Swiss albino mice. Immunostaining for PCNA and ki-67 was used to mark proliferating cells in tissues. Haematoxylin and eosin staining and toluidine staining were employed to assess inflammation, and TUNEL assay was used to detect apoptosis in tissues. The signalling events were evaluated using Western blot, imunohistochemistry and immunofluorescence staining. MTT assay and clonogenic assay were performed to assess the viability and proliferation of cancer cells, in vitro.

resultsIn mice, topical application of tryptanthrin suppressed skin carcinogenesis. It attenuated inflammation, impeded the proliferation of hair follicle (HF) cells and suppressed the activation of β-catenin, a major driver of HF cell proliferation. Additionally tryptanthrin suppressed the activation of ERK1/2 and p38, both of which promote β-catenin activation and lowered the expression of c-Myc and cyclin-D1. Tryptanthrin suppressed the proliferation of the human NMSC cell line, A431 and abrogated EGF-induced activation of β-catenin and subsequent cytoskeletal rearrangement.

conclusionThe study demonstrates with molecular evidence that tryptanthrin is an effective suppressor of NMSC.

Indexed as

AnimalsDrug Screening Assays, Antitumorgamma-Aminobutyric AcidKi-67 AntigenMiceNeoplasm ProteinsProliferating Cell Nuclear AntigenQuinazolinesSkin NeoplasmsTetradecanoylphorbol Acetate4-(dimethylamino)butyric acidgamma-Aminobutyric AcidKi-67 AntigenMki67 protein, mouseNeoplasm ProteinsProliferating Cell Nuclear AntigenQuinazolinesTetradecanoylphorbol Acetatetryptanthrinemultistage carcinogenesis modelpre-clinical studyskin cancerTryptanthrin

Identifiers

PMID31663659
PMCPMC6985671
OpenAlexW2982456950

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.