Evidence map›Paper›PMID 28359741›Full record

ReviewBiochimica et biophysica acta. Reviews on cancer2017

Targeting the mercapturic acid pathway and vicenin-2 for prevention of prostate cancer.

Sharad S Singhal, Divya Jain, Preeti Singhal, Sanjay Awasthi, Jyotsana Singhal, David Horne

Open access · bronzeAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta. Reviews on cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Review
  3. Antinociceptive Effect ofLife (Basel, Switzerland) · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Life (Basel, Switzerland) · 2023
    Article
  8. Article
  9. Anticancer Potential ofBioinformatics and biology insights · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Structure Identification of ViceninII Extracted fromMolecules (Basel, Switzerland) · 2019
    Article
  14. Article
  15. 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

6 authors at 4 institutions in 2 countries.

Sharad S SinghalDepartment of Molecular Medicine, Beckman Research Institute of City of Hope, Comprehensive Cancer Center and National Medical Center, Duarte, CA 91010, United States. Electronic address: ssinghal@coh.org.
Divya JainDepartment of Ophthalmology, University College of Medical Sciences and Guru Teg Bahadur Hospital, New Delhi 110095, India.
Preeti SinghalUniversity of Texas Health, San Antonio, TX 78229, United States.
Sanjay AwasthiTexas Tech University Health Sciences Center, Lubbock, TX 79430, United States.
Jyotsana SinghalDepartment of Molecular Medicine, Beckman Research Institute of City of Hope, Comprehensive Cancer Center and National Medical Center, Duarte, CA 91010, United States.
David HorneDepartment of Molecular Medicine, Beckman Research Institute of City of Hope, Comprehensive Cancer Center and National Medical Center, Duarte, CA 91010, United States.
City Of Hope National Medical Center · USTexas Tech University · USThe University of Texas Health Science Center at San Antonio · USUniversity College of Medical Sciences · IN

Funding

MECHANISM OF DRUG TRANSPORT IN LUNG CANCER CELLSR01CA077495 · NCI · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI AWASTHI, SANJAY · 1998 to 2011
$2.8M
NCI NIH HHS R01 CA077495
6 · The paper itself

Abstract

Prostate cancer (CaP) is often androgen-sensitive malignancy and regresses upon inhibition of androgen signaling. However, CaP, nearly always develops androgen resistance and progresses to aggressive and lethal androgen-independent CaP, which lacks satisfactory therapy. For metastatic CaP, patients are often treated with Taxotere (docetaxel), a cytoskeleton-targeted chemotherapy drug, that provides transient palliative benefit but to which patients rapidly develop drug-resistance. Combination chemotherapy may be used instead, but is more toxic and adds little clinically relevant benefit over docetaxel. Therefore, novel strategies to enhance docetaxel efficacy are needed to effectively treat patients with metastatic CaP. The mercapturic acid pathway, which metabolizes genotoxic and pro-apoptotic toxins, is over-expressed in CaP and plays an important role in carcinogenesis, metastasis and therapy-resistance of CaP. Vicenin-2, a flavonoid derived from Tulsi (holy basil) as an active compound, inhibits the growth of CaP and increases the anti-tumor activity of docetaxel in-vitro and in-vivo. Taken together, the combination of vicenin-2 and docetaxel could be highly effective in the treatment of advanced and metastatic CaP due to their multi-targeting anti-tumor potential.

Indexed as

AcetylcysteineAnimalsAntineoplastic AgentsApigeninDocetaxelDrug Resistance, NeoplasmGlucosidesHumansMaleProstatic NeoplasmsSignal TransductionTaxoidsAcetylcysteineAntineoplastic AgentsApigeninapigenin-6,8-di-C-glycopyranosideDocetaxelGlucosidesTaxoidsClathrin-dependent endocytosisDrug-resistanceGlutathione-conjugate transportProstate cancerRLIP76 (RalBP1)Vicenin

Identifiers

PMID28359741
PMCPMC5638116
OpenAlexW2600770628

What OpenQuestion holds

Textmetadata
LicenceTDM
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.