Evidence map›Paper›PMID 35566385›Full record

ReviewMolecules (Basel, Switzerland)2022

A Review on Mechanistic Insight of Plant Derived Anticancer Bioactive Phytocompounds and Their Structure Activity Relationship.

Kishor Mazumder, Asma Aktar, Priyanka Roy, Biswajit Biswas, Md Emran Hossain, Kishore Kumar Sarkar, Sitesh Chandra Bachar, Firoj Ahmed, A S M Monjur-Al-Hossain, Koichi Fukase

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–field-weighted citation impact
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

38 citing papers in PubMed.

  1. Article
  2. Mechanistic Insights intoInternational journal of molecular sciences · 2026
    Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Oncology Clinical Trials Targeting Members of the Cadherin Superfamily: A Review.Journal of immunotherapy and precision oncology · 2025
    Review
  16. Review
  17. Review
  18. Article
  19. Pharmaceuticals (Basel, Switzerland) · 2024
    Article
  20. Phytochemicals in Drug Discovery-A Confluence of Tradition and Innovation.International journal of molecular sciences · 2024
    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

10 authors.

Kishor MazumderDepartment of Pharmacy, Jashore University of Science and Technology, Jashore 7408, Bangladesh.ORCID 0000-0002-8711-7409
Asma AktarDepartment of Pharmacy, Jashore University of Science and Technology, Jashore 7408, Bangladesh.
Priyanka RoyDepartment of Pharmacy, Jashore University of Science and Technology, Jashore 7408, Bangladesh.
Biswajit BiswasDepartment of Pharmacy, Jashore University of Science and Technology, Jashore 7408, Bangladesh.ORCID 0000-0002-2948-2256
Md Emran HossainDepartment of Pharmacy, Jashore University of Science and Technology, Jashore 7408, Bangladesh.
Kishore Kumar SarkarDepartment of Pharmacy, Jashore University of Science and Technology, Jashore 7408, Bangladesh.ORCID 0000-0001-6127-6412
Sitesh Chandra BacharDepartment of Pharmacy, Faculty of Pharmacy, University of Dhaka, Dhaka 1207, Bangladesh.
Firoj AhmedDepartment of Pharmacy, Faculty of Pharmacy, University of Dhaka, Dhaka 1207, Bangladesh.ORCID 0000-0003-0690-1451
A S M Monjur-Al-HossainDepartment of Pharmaceutical Technology, Faculty of Pharmacy, University of Dhaka, Dhaka 1207, Bangladesh.ORCID 0000-0001-5585-7763
Koichi FukaseDepartment of Chemistry, Graduate School of Science, Osaka University, 1-1 Machikaneyama, Toyonaka, Osaka 560-0043, Japan.ORCID 0000-0001-8844-0710

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a disorder that rigorously affects the human population worldwide. There is a steady demand for new remedies to both treat and prevent this life-threatening sickness due to toxicities, drug resistance and therapeutic failures in current conventional therapies. Researchers around the world are drawing their attention towards compounds of natural origin. For decades, human beings have been using the flora of the world as a source of cancer chemotherapeutic agents. Currently, clinically approved anticancer compounds are vincristine, vinblastine, taxanes, and podophyllotoxin, all of which come from natural sources. With the triumph of these compounds that have been developed into staple drug products for most cancer therapies, new technologies are now appearing to search for novel biomolecules with anticancer activities. Ellipticine, camptothecin, combretastatin, curcumin, homoharringtonine and others are plant derived bioactive phytocompounds with potential anticancer properties. Researchers have improved the field further through the use of advanced analytical chemistry and computational tools of analysis. The investigation of new strategies for administration such as nanotechnology may enable the development of the phytocompounds as drug products. These technologies have enhanced the anticancer potential of plant-derived drugs with the aim of site-directed drug delivery, enhanced bioavailability, and reduced toxicity. This review discusses mechanistic insights into anticancer compounds of natural origins and their structural activity relationships that make them targets for anticancer treatments.

Indexed as

Antineoplastic AgentsNeoplasmsHumansPlantsPodophyllotoxinStructure-Activity RelationshipAntineoplastic AgentsPodophyllotoxinanticancer bioactive phytocompoundscytotoxic agentsneoplastic diseaseproliferationstructure activity relationship (SAR)

Identifiers

PMID35566385
PMCPMC9102595

What Socratic 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 Socratic graph.