Evidence map›Paper›PMID 29183320›Full record

ArticleBMC complementary and alternative medicine2017

Fungal 7-epi-10-deacetyltaxol produced by an endophytic Pestalotiopsis microspora induces apoptosis in human hepatocellular carcinoma cell line (HepG2).

Kamalraj Subban, Satpal Singh, Ramesh Subramani, Muthumary Johnpaul, Jayabaskaran Chelliah

Open access · goldAbstract read
In one paragraph

Article in BMC complementary and alternative medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-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

6 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Pest categorisation ofEFSA journal. European Food Safety Authority · 2023
    Article
  5. Insights into Taxol® biosynthesis by endophytic fungi.Applied microbiology and biotechnology · 2023
    Review
  6. Molecules (Basel, Switzerland) · 2022
    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

5 authors at 3 institutions in 2 countries.

Kamalraj SubbanDepartment of Biochemistry, Indian Institute of Science, Bangalore, Karnataka, 560012, India.
Satpal SinghDepartment of Biochemistry, Indian Institute of Science, Bangalore, Karnataka, 560012, India.
Ramesh SubramaniDepartment of Biology, College of Engineering, Science & Technology, Fiji National University, Natabua Campus, Lautoka, Fiji Islands.
Muthumary JohnpaulCentre for Advanced Studies in Botany, University of Madras, Guindy Campus, Chennai, Tamil Nadu, India.
Jayabaskaran ChelliahDepartment of Biochemistry, Indian Institute of Science, Bangalore, Karnataka, 560012, India. cjb@biochem.iisc.ernet.in.
Indian Institute of Science Bangalore · INUniversity of Madras · INFiji National University · FJ

Funding

Department of Science & technology, GOI, New Delhi, India EMR/2015/001071
6 · The paper itself

Abstract

backgroundPaclitaxel (taxol) is a potent anticancer drug that is used in the treatment of a wide variety of cancerous. In the present study, we identified a taxol derivative named 7-epi-10-deacetyltaxol (EDT) from the culture of an endophytic fungus Pestalotiopsis microspora isolated from the bark of Taxodium mucronatum. This study was carried out to investigate the effects of fungal EDT on cell proliferation, the induction of apoptosis and the molecular mechanisms of apoptosis in human hepatoma HepG2 cells in vitro.

methodsThe endophytic fungus was identified by traditional and molecular taxonomical characterization and the fungal EDT was purified using column chromatography and confirmed by various spectroscopic and chromatographic comparisons with authentic paclitaxel. We studied the in vitro effects of EDT on HepG2 cells for parameters such as cell cycle distribution, DNA fragmentation, reactive oxygen species (ROS) generation and nuclear morphology. Further, western blot analysis was used to evaluate Bcl-2-associated X protein (Bax), B-cell lymphoma 2 (Bcl-2), p38-mitogen activated protein kinase (MAPK) and poly [ADP-ribose] polymerase (PARP) expression.

resultsWe demonstrate that the fungal EDT exhibited significant in vitro cytotoxicity in HepG2 cells. We investigated cytotoxicity mechanism of EDT in HepG2 cells. The results showed nuclear condensation and DNA fragmentation were observed in cells treated with fungal EDT. Besides, the fungal EDT arrested HepG2 cells at G2/M phase of cell cycle. Furthermore, fungal EDT induced apoptosis in HepG2 cells in a dose-dependent manner associated with ROS generation and increased Bax/Bcl-2 ratio, p38 MAPKs and PARP cleavage.

conclusionsOur data show that EDT induced apoptotic cell death in HepG2 cells occurs through intrinsic pathway by generation of ROS mediated and activation of MAPK pathway. This is the first report for 7-epi-10-deacetyltaxol (EDT) isolated from a microbial source.

Indexed as

Antineoplastic AgentsApoptosisCarcinoma, HepatocellularCell CycleCell SurvivalEndophytesHep G2 CellsHumansLiver NeoplasmsReactive Oxygen SpeciesTaxoidsXylariales10-deacetyltaxolAntineoplastic AgentsReactive Oxygen SpeciesTaxoids7-epi-10-deacetyltaxol (EDT)ApoptosisEndophyteG2/M arrestPestalotiopsis

Identifiers

PMID29183320
PMCPMC5706334
OpenAlexW2770280942

What OpenQuestion holds

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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.