Evidence mapPaperPMID 38201944Full record

ArticleNutrients2023

Mechanism of Antitumor Effects of Saffron in Human Prostate Cancer Cells.

Mohammad Khan, Kaitlyn Hearn, Christian Parry, Mudasir Rashid, Hassan Brim, Hassan Ashktorab, Bernard Kwabi-Addo

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Review
  3. Epigenomics Nutritional Insights ofInternational journal of molecular sciences · 2025
    Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. 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

7 authors at 2 institutions in 1 country.

Mohammad KhanDepartment of Biochemistry and Molecular Biology, Howard University, Washington, DC 20059, USA.
Kaitlyn HearnDepartment of Life Sciences, Xavier University of Louisiana, New Orleans, LA 70125, USA.
Christian ParryDepartment of Microbiology, Howard University, Washington, DC 20059, USA.
Mudasir RashidCancer Center, Howard University, Washington, DC 20059, USA.
Hassan BrimDepartment of Pathology, Howard University, Washington, DC 20059, USA.
Hassan AshktorabCancer Center, Howard University, Washington, DC 20059, USA.ORCID 0000-0002-4048-4666
Bernard Kwabi-AddoDepartment of Biochemistry and Molecular Biology, Howard University, Washington, DC 20059, USA.
Howard University · USXavier University of Louisiana · US

Funding

Sleep Disorders in Adults with Sickle Cell Disease: Frequency, Associations with Cardiovascular and Pain Indicators, and Responses to TreatmentU54MD007597 · NIMHD · HOWARD UNIVERSITY · 2022 to 2025
$12.8M
NIH HHS 2U54MD007597NIMHD NIH HHS U54 MD007597
6 · The paper itself

Abstract

Prostate cancer is the most common cancer and the second leading cause of cancer deaths among men in the USA. Several studies have demonstrated the antitumor properties of saffron in different types of cancers, including prostate cancer. The oral administration of saffron extract has been reported to have antitumor effects on aggressive prostate-cancer-cell-line-derived xenografts in nude male mice. The objective of this study was to carry out in vitro studies of saffron-treated prostate cancer cells to ascertain the effects of saffron on key intermediates in prostate carcinogenesis. Our studies demonstrated the significant inhibition of cell proliferation for androgen-sensitive prostate cancer cell lines via apoptotic pathways. We also demonstrate the statistically significant down-regulation of DNA methyltransferases (COMT, MGMT, EHMT2, and SIRT1 deacetylase) in saffron-treated prostate cancer cells. In addition, saffron-treated prostate cancer cells displayed a statistically significant dysregulation of DNA repair intermediates (WRN, p53, RECQ5, MST1R, and WDR70) in a time-dependent manner. Furthermore, Western blot analysis demonstrated that saffron treatment induced changes in the expression of other key genes (DNMT1, DNMT3b, MBD2, CD44, HDAC3, c-Myc, NF-kB, TNFα, AR, N-RAS, and PTEN) in prostate cancer cells. Collectively, our findings demonstrate the important mechanisms by which saffron mediates anti-tumor properties in prostate cancer. These findings suggest that the use of saffron supplements alongside standard treatment protocols may yield beneficial effects for individuals with prostate cancer.

Indexed as

Biological ProductsCrocusProstatic NeoplasmsAdministration, OralAnimalsDNA-Binding ProteinsHistocompatibility AntigensHistone-Lysine N-MethyltransferaseHumansMaleMiceProstateTumor Necrosis Factor-alphaBiological ProductsDNA-Binding ProteinsEHMT2 protein, humanHistocompatibility AntigensHistone-Lysine N-MethyltransferaseMBD2 protein, humanTumor Necrosis Factor-alphaanti-tumorDNA repair genesepigeneticsprostate cancer cell linessaffron

Identifiers

PMID38201944
PMCPMC10780623
OpenAlexW4390348299

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.