Evidence map›Paper›PMID 25879420›Full record

ArticleJournal of biomedical science2015

Shikonin selectively induces apoptosis in human prostate cancer cells through the endoplasmic reticulum stress and mitochondrial apoptotic pathway.

Rishi Kumar Gara, Vikas Kumar Srivastava, Shivali Duggal, Jaspreet Kaur Bagga, Mlb Bhatt, Sabyasachi Sanyal, Durga Prasad Mishra

Open access · diamondAbstract read
In one paragraph

Article in Journal of biomedical science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

39 citing papers in PubMed, 73 citations in OpenAlex.

  1. Review
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  4. GenusPlants (Basel, Switzerland) · 2025
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  7. Pharmacological Significance ofFoods (Basel, Switzerland) · 2024
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  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Promising Nanomedicines of Shikonin for Cancer Therapy.International journal of nanomedicine · 2023
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Food science & nutrition · 2021
    Article
  19. Article
  20. Shikonin Derivatives fromNutrients · 2021
    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

7 authors at 3 institutions in 2 countries.

Rishi Kumar GaraCell Death Research Laboratory, Endocrinology Division CSIR-Central Drug Research Institute, Lucknow, 226031, India. rgara@uthsc.edu.
Vikas Kumar SrivastavaDepartment of Radiotherapy, King George Medical University, Lucknow, 226003, India. vikaskgmu@gmail.com.
Shivali DuggalDepartment of Radiotherapy, King George Medical University, Lucknow, 226003, India. shivalivi@gmail.com.
Jaspreet Kaur BaggaCell Death Research Laboratory, Endocrinology Division CSIR-Central Drug Research Institute, Lucknow, 226031, India. jaspreet.cdri@gmail.com.
Mlb BhattDepartment of Radiotherapy, King George Medical University, Lucknow, 226003, India. drmlbhatt@yahoo.com.
Sabyasachi SanyalDivision of Biochemistry, CSIR-Central Drug Research Institute, Lucknow, 226031, India. s_sanyal@cdri.res.in.
Durga Prasad MishraCell Death Research Laboratory, Endocrinology Division CSIR-Central Drug Research Institute, Lucknow, 226031, India. dpm@cdri.res.in.
Central Drug Research Institute · INKing George's Medical University · INUniversity of Tennessee Health Science Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite the recent progress in screening and therapy, a majority of prostate cancer cases eventually attain hormone refractory and chemo-resistant attributes. Conventional chemotherapeutic strategies are effective at very high doses for only palliative management of these prostate cancers. Therefore chemo-sensitization of prostate cancer cells could be a promising strategy for increasing efficacy of the conventional chemotherapeutic agents in prostate cancer patients. Recent studies have indicated that the chemo-preventive natural agents restore the pro-apoptotic protein expression and induce endoplasmic reticulum stress (ER stress) leading to the inhibition of cellular proliferation and activation of the mitochondrial apoptosis in prostate cancer cells. Therefore reprogramming ER stress-mitochondrial dependent apoptosis could be a potential approach for management of hormone refractory chemoresistant prostate cancers. We aimed to study the effects of the natural naphthoquinone Shikonin in human prostate cancer cells.

resultsThe results indicated that Shikonin induces apoptosis in prostate cancer cells through the dual induction of the endoplasmic reticulum stress and mitochondrial dysfunction. Shikonin induced ROS generation and activated ER stress and calpain activity. Moreover, addition of antioxidants attenuated these effects. Shikonin also induced the mitochondrial apoptotic pathway mediated through the enhanced expression of the pro-apoptotic Bax and inhibition of Bcl-2, disruption of the mitochondrial membrane potential (MMP) followed by the activation of caspase-9, caspase-3, and PARP cleavage.

conclusionThe results suggest that shikonin could be useful in the therapeutic management of hormone refractory prostate cancers due to its modulation of the pro-apoptotic ER stress and mitochondrial apoptotic pathways.

Indexed as

Antineoplastic AgentsApoptosisCell Line, TumorCell ProliferationEndoplasmic Reticulum StressHumansMaleMembrane Potential, MitochondrialMitochondriaNaphthoquinonesProstatic NeoplasmsAntineoplastic AgentsNaphthoquinonesshikonin

Identifiers

PMID25879420
PMCPMC4389804
OpenAlexW2108175962

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.