Evidence map›Paper›PMID 34907713›Full record

ArticleJournal of applied biomedicine2021

GC-MS Metabolomics profiling and HR-APCI-MS characterization of potential anticancer compounds and antimicrobial activities of extracts from Picrorhiza kurroa roots.

Qudsia Tabassam, Tahir Mehmood, Sibtain Ahmed, Shagufta Saeed, Abdul Rauf Raza, Farooq Anwar

Open access · goldAbstract read
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In one paragraph

Article in Journal of applied biomedicine, 2021. 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
2.0field-weighted citation impact, top 13% 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, 14 citations in OpenAlex.

  1. Review
  2. Plant Metabolomics: The Future of Anticancer Drug Discovery.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  3. Article
  4. Article
  5. Biological Activity ofInternational journal of molecular sciences · 2022
    Article
  6. 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

6 authors at 3 institutions in 2 countries.

Qudsia TabassamUniversity of Sargodha, Institute of Chemistry, Sargodha-40100, Pakistan.
Tahir MehmoodUniversity of Sargodha, Institute of Chemistry, Sargodha-40100, Pakistan.
Sibtain AhmedUniversity of California San Diego, 9500 Gilman Drive La Jolla, CA 92093, USA.
Shagufta SaeedUniversity of Veterinary and Animal Sciences-UVAS, Institute of Biochemistry and Biotechnology, 54000-Lahore, Pakistan.
Abdul Rauf RazaUniversity of Sargodha, Institute of Chemistry, Sargodha-40100, Pakistan.
Farooq AnwarUniversity of Sargodha, Institute of Chemistry, Sargodha-40100, Pakistan.
University of Sargodha · PKUniversity of California, San Diego · USUniversity of Veterinary and Animal Sciences · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study explores pharmacological potential and phytochemicals profiling of Picrorhiza kurroa extracts against mammalian cancer cell lines and pathogenic microbes. Bioactive extracts from roots of Picrorhiza kurroa were recovered in the methanol, 50% aqueous dichloromethane (50 : 50 v/v) and n-hexane. Antimicrobial activity of the bioactive extracts was assessed against selected strains of bacteria and pathogenic fungi. Aqueous dichloromethane extract showed highest zone of growth inhibition (39.06 ± 1.0 mm) towards Staphylococcus aureus bacteria while methanolic extract showed the lowest inhibition (6.3 ± 4.1 mm) to Escherichia coli bacteria. The tested extracts such as methanol and aqueous dichloromethane exhibited higher inhibition antifungal activity against Aspergillus flavus compared to Fusarium oxysporum. As far as cytotoxicity (MTT assay) of the tested extracts is concerned, n-hexane and aqueous dichloromethane extracts were found to be very active against all cancer cell lines (breast cancer MCF7, MDA-MB-231, SKBR3 and ovarian cancer SKOV3). A preliminary phytochemicals profiling was performed in extracts using GC-MS. Several fractions of active extract were separated with HPLC and analyzed using High Resolution Atmospheric Pressure Chemical Ionization Mass Spectrometry (HR-APCI-MS). Two purified compounds (Dihydromikanolide and 1,3-Dicyclohexyl-4-(cyclohexylimino)-2-(cyclohexylethylamino)-3,4-dihydro-1,3-diazetium) were further evaluated for their anticancer activity against ovarian cancer cell line. Our findings depict that all the tested extracts showed considerable anticancer potential through cell viability assays. The purified compound 1 - Dihydromikanolide from methanolic extract was found to be active against ovarian cancer cells and can be explored as a promising nutra-pharmaceutical candidate against ovarian cancer. However, further studies exploring the molecular pathways and in vivo testing are required.

Indexed as

Anti-Infective AgentsOvarian NeoplasmsPicrorhizaAnimalsAtmospheric PressureFemaleGas Chromatography-Mass SpectrometryHumansMammalsMetabolomicsMethanolMethylene ChloridePhytochemicalsPlant ExtractsAnti-Infective AgentsMethanolMethylene ChloridePhytochemicalsPlant ExtractsAntimicrobial agentsBioactive extractsCell viability assayCytotoxicityGC-MSHR-APCI-MSOvarian cancerPhytochemicals

Identifiers

PMID34907713
OpenAlexW3121709564

What OpenQuestion holds

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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.