Evidence map›Paper›PMID 30560046›Full record

ArticleCurrent pharmacology reports2018

Role of Dietary Cancer-Preventive Phytochemicals in Pancreatic Cancer Stem Cells.

Gaurav Kumar, Mudassir Farooqui, Chinthalapally V Rao

Abstract read
In one paragraph

Article in Current pharmacology reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Dietary Phytochemicals Targeting Cancer Stem Cells.Molecules (Basel, Switzerland) · 2019
    Review
  6. Frontiers in bioengineering and biotechnology · 2019
    Article
  7. 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

3 authors at 1 institution in 1 country.

Gaurav KumarCenter for Cancer Prevention and Drug Development, Department of Medicine, Hematology/Oncology, The University of Oklahoma Health Sciences Center, and VA Medical Center, Oklahoma City, United States.
Mudassir FarooquiCenter for Cancer Prevention and Drug Development, Department of Medicine, Hematology/Oncology, The University of Oklahoma Health Sciences Center, and VA Medical Center, Oklahoma City, United States.
Chinthalapally V RaoCenter for Cancer Prevention and Drug Development, Department of Medicine, Hematology/Oncology, The University of Oklahoma Health Sciences Center, and VA Medical Center, Oklahoma City, United States.
University of Oklahoma Health Sciences Center · US

Funding

Safer Approaches to CRC ChemopreventionR01CA213987 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI RAO, CHINTHALAPALLY V. · 2017 to 2021
$2.4M
Targeting mPGES-1/5-LOX for Prevention of CRC in High-Risk VeteransI01BX003198 · VA · OKLAHOMA CITY VA MEDICAL CENTER · PI RAO, CHINTHALAPALLY V. · 2016 to 2020
–
BLRD VA I01 BX003198NCI NIH HHS HHSN261201200013INCI NIH HHS N01 CN053300NCI NIH HHS R01 CA213987
6 · The paper itself

Abstract

purpose of reviewThis article provides a brief overview of cancer-preventive phytochemicals specifically targeting pancreatic cancer (PC) stem cells for prevention and treatment. RECENT

findingsCancer stem cells (CSCs) represent a small proportion of the total cells of a given tumor, and contribute to tumor growth, recurrence, metastasis, and treatment resistance. Many intertwined pathways, including hedgehog, Wnt Signaling, and NOTCH, have been shown to play a role in the formation of CSCs. Recently, numerous chemopreventive agents, such as genistein, (-)-epigallocatechin-3-gallate (EGCG), sulforaphane, curcumin, resveratrol, and quercetin, have been shown to target CSCs mediated through the inhibition of multiple signalling pathways, to avoid toxicity and the side effects of chemical compounds. SUMMARY: A growing body of research suggests that CSCs are the drivers in treatment resistance, cancer recurrence, and metastasis, in addition to tumor initiation and heterogeneity. Patient survival depends on these CSCs, which are one cause of tumor recurrence after surgery and chemotherapy. Therefore, target selection; an improved understanding of CSC biology, the genetic and molecular profiles of CSCs, and their key signaling pathways, and; appropriate clinical trials endpoints that are designed to target CSCs will help in the development of drugs that will specifically target this small population of stem cells.

Indexed as

cancer stem cellspancreatic cancerphytochemicalspolyphenols

Identifiers

PMID30560046
PMCPMC6294462
OpenAlexW2809938448

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.