Evidence map›Paper›PMID 32291806›Full record

ArticleMolecular carcinogenesis2020

A novel terpenoid class for prevention and treatment of KRAS-driven cancers: Comprehensive analysis using in situ, in vitro, and in vivo model systems.

Arsheed A Ganaie, Hifzur R Siddique, Ishfaq A Sheikh, Aijaz Parray, Lei Wang, Jayanth Panyam, Peter W Villalta, Yibin Deng, Badrinath R Konety, Mohammad Saleem

Open access · greenAbstract read
In one paragraph

Article in Molecular carcinogenesis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
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  4. Review
  5. Deciphering Neuroprotective Effect ofCurrent drug targets · 2024
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  8. Phytochemical Screening ofPlants (Basel, Switzerland) · 2022
    Article
  9. Intranasal Iloprost Prevents Tumors in a Murine Lung Carcinogenesis Model.Cancer prevention research (Philadelphia, Pa.) · 2022
    Article
  10. 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 at 2 institutions in 4 countries.

Arsheed A GanaieDepartment of Urology, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Hifzur R SiddiqueDepartment of Urology, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Ishfaq A SheikhKing Fahd Medical Research Center, King Abdulaziz University, Jeddah, Saudi Arabia.
Aijaz ParrayDepartment of Urology, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Lei WangHormel Institute, University of Minnesota, Austin, Minnesota.
Jayanth PanyamSchool of Pharmacy, University of Minnesota, Minneapolis, Minnesota.
Peter W VillaltaAnalytical Chemistry Core, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Yibin DengDepartment of Urology, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Badrinath R KonetyDepartment of Urology, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Mohammad SaleemDepartment of Urology, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-7422-7967
University of Minnesota · USKing Abdulaziz University · SA

Funding

Novel targeted chemo/immunotherapy approach for localized and metastatic CaPR01CA193739 · NCI · UNIVERSITY OF MINNESOTA · PI BHAT, MOHAMMAD SALEEM · 2016 to 2020
$1.8M
NCI NIH HHS R01 CA193739
6 · The paper itself

Abstract

Inhibiting the disease progression in KRAS-driven cancers after diagnosis has been a difficult task for clinicians to manage due to the lack of effective intervention/preventive therapies. KRAS-driven cancers depend on sustained KRAS signaling. Although developing inhibitors of KRAS signaling has proven difficult in the past, the quest for identifying newer agents has not stopped. Based on studies showing terpenoids as modulators of KRAS-regulated downstream molecular pathways, we asked if this chemical family has an affinity of inhibiting KRAS protein activity. Using crystal structure as a bait in silico, we identified 20 terpenoids for their KRAS protein-binding affinity. We next carried out biological validation of in silico data by employing in situ, in vitro, patient-derived explant ex vivo, and KPC transgenic mouse models. In this report, we provide a comprehensive analysis of a lup-20(29)-en-3b-ol (lupeol) as a KRAS inhibitor. Using nucleotide exchange, isothermal titration calorimetry, differential scanning fluorimetry, and immunoprecipitation assays, we show that lupeol has the potential to reduce the guanosine diphosphate/guanosine triphosphate exchange of KRAS protein including mutant KRAS

Indexed as

Disease Models, AnimalAnimalsAnti-Inflammatory AgentsApoptosisCell ProliferationCell Transformation, NeoplasticDisease ProgressionFemaleHumansIn Vitro TechniquesLupanesMiceMice, Inbred C57BLMice, TransgenicPancreatic NeoplasmsPentacyclic TriterpenesAnti-Inflammatory AgentsKRAS protein, humanLupaneslupeolPentacyclic TriterpenesProto-Oncogene Proteins p21(ras)colon cancerKRASG12Dlung cancerpancreatic cancertransgenic mice

Identifiers

PMID32291806
PMCPMC7334075
OpenAlexW3015589167

What OpenQuestion holds

Textmetadata
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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.