Evidence map›Paper›PMID 27782823›Full record

ArticleBMC complementary and alternative medicine2016

Pro-apoptotic and cytotoxic effects of enriched fraction of Elytranthe parasitica (L.) Danser against HepG2 Hepatocellular carcinoma.

Nimmy Kumar, Subhankar Biswas, Asha Elizabeth Mathew, Subin Varghese, Jessy Elizabeth Mathew, K Nandakumar, Jesil Mathew Aranjani, Richard Lobo

Open access · goldAbstract read
In one paragraph

Article in BMC complementary and alternative medicine, 2016. 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
4.8field-weighted citation impact, top 6% 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, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Telomerase Inhibitors from Natural Products and Their Anticancer Potential.International journal of molecular sciences · 2017
    Review
  6. 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

8 authors at 1 institution in 1 country.

Nimmy KumarDepartment of Pharmacognosy, Manipal College of Pharmaceutical Sciences, Manipal University, Manipal, 576 104, Karnataka, India.
Subhankar BiswasDepartment of Pharmacology, Manipal College of Pharmaceutical Sciences, Manipal University, Manipal, 576 104, Karnataka, India.
Asha Elizabeth MathewDepartment of Pharmacology, Manipal College of Pharmaceutical Sciences, Manipal University, Manipal, 576 104, Karnataka, India.
Subin VargheseDepartment of Pharmacology, Manipal College of Pharmaceutical Sciences, Manipal University, Manipal, 576 104, Karnataka, India.
Jessy Elizabeth MathewDepartment of Pharmaceutical Chemistry, Manipal College of Pharmaceutical Sciences, Manipal University, Manipal, 576 104, Karnataka, India.
K NandakumarDepartment of Pharmacology, Manipal College of Pharmaceutical Sciences, Manipal University, Manipal, 576 104, Karnataka, India.
Jesil Mathew AranjaniDepartment of Pharmaceutical Biotechnology, Manipal College of Pharmaceutical Sciences, Manipal University, Manipal, 576 104, Karnataka, India.
Richard LoboDepartment of Pharmacognosy, Manipal College of Pharmaceutical Sciences, Manipal University, Manipal, 576 104, Karnataka, India. avemaria_lobo@yahoo.com.
Manipal Academy of Higher Education · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC), the most common type of liver cancer accounts for more than one million deaths worldwide. Current treatment modality for HCC is marginally effective. Plants belonging to Mistletoe family (Loranthaceae) have been used in chemotherapy for many years. The present study was aimed at exploring the anti-proliferative, pro-oxidant and pro-apoptotic potential of stem of Elytranthe parasitica (L.) Danser (EP), a parasitic shrub belonging to Loranthaceae.

methodsElytranthe parasitica (L.) Danser, a climbing parasitic shrub was investigated for its cytotoxic activity against HepG2, a hepatocellular carcinoma cell line by Sulforhodamine B (SRB) assay. Further, pro-oxidant activity of EP extract/fractions was studied using copper phenanthroline assay. To understand the mechanism of cell death, the pro-apoptotic effects of Hep-G2 cells treated with EP extract/fractions were visualized by dual staining using acridine orange and ethidium bromide, a morphological marker of apoptosis. Phytochemical profiling of EP was explored by estimating the phenol, flavonoid and tannin content in its various fractions and extract. The occurrence of gallic acid, a principal polyphenol in EP extract and fractions was detected and further quantified using HPTLC (High Performance Thin Layer Chromatography) fingerprinting.

resultActive fraction of Elytranthe parasitica, EP.DEE exhibited potent cytotoxic activity in a dose dependent manner against HepG2 hepatocellular carcinoma cell line with an IC50 of 56.7 ± 7.8 μg/mL. Dual staining with acridine orange and ethidium bromide revealed that HepG2 cells treated with EP active fractions underwent cell death chiefly by apoptosis. Highest phenol, flavonoid and tannin content were observed in active fractions, EP.EA (Ethyl acetate fraction) and EP.DEE (Diethyl ether fraction). Gallic acid was identified and quantified in EP extract and active fractions, EP.DEE and EP.EA.

conclusionOur findings indicate EP active fraction could be a promising contender in the treatment of hepatocellular carcinoma.

Indexed as

Antineoplastic Agents, PhytogenicPlant ExtractsApoptosisCarcinoma, HepatocellularCell SurvivalGallic AcidHep G2 CellsHumansLiver NeoplasmsPhenolsTanninsTracheophytaAntineoplastic Agents, PhytogenicGallic AcidPhenolsPlant ExtractsTanninsAnti-proliferativeApoptosisElytranthe parasiticaGallic acidHepatocellular carcinomaHepG2Phytochemical

Identifiers

PMID27782823
PMCPMC5080845
OpenAlexW2535737599

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.