Evidence map›Paper›PMID 34499267›Full record

ReviewCancer metastasis reviews2021

Targeting KRAS in pancreatic cancer: new drugs on the horizon.

Sahar F Bannoura, Md Hafiz Uddin, Misako Nagasaka, Farzeen Fazili, Mohammed Najeeb Al-Hallak, Philip A Philip, Bassel El-Rayes, Asfar S Azmi

Open access · greenAbstract readReview
In one paragraph

Review in Cancer metastasis reviews, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
5.9field-weighted citation impact, top 2% 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

65 citing papers in PubMed, 94 citations in OpenAlex.

  1. Unravelling the pathogenesis and therapeutic approaches of pancreatic ductal adenocarcinoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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  12. Impact ofHealth science reports · 2025
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5 more citing papers are in PubMed but not listed here.

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

8 authors at 3 institutions in 1 country.

Sahar F BannouraDepartment of Oncology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
Md Hafiz UddinDepartment of Oncology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
Misako NagasakaDivision of Hematology/Oncology, Department of Medicine, UCI Health, Orange, CA, 92868, USA.
Farzeen FaziliDepartment of Oncology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
Mohammed Najeeb Al-HallakDepartment of Oncology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
Philip A PhilipDepartment of Oncology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
Bassel El-RayesWinship Cancer Institute, Emory University, Atlanta, GA, 30322, USA.
Asfar S AzmiDepartment of Oncology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, 48201, USA. azmia@karmanos.org.
The Barbara Ann Karmanos Cancer Institute · USWayne State University · USEmory University · US

Funding

Clinical Translation of Nuclear Export Inhibitor in Metastatic Pancreatic CancerR37CA215427 · NCI · WAYNE STATE UNIVERSITY · PI AZMI, ASFAR S · 2018 to 2024
$2.4M
A novel therapy for pancreatic neuroendocrine tumorsR01CA240607 · NCI · WAYNE STATE UNIVERSITY · PI AZMI, ASFAR S, EL-RAYES, BASSEL · 2020 to 2024
$1.7M
NCI NIH HHS R01 CA240607NCI NIH HHS R37 CA215427
6 · The paper itself

Abstract

Kirsten Rat Sarcoma (KRAS) is a master oncogene involved in cellular proliferation and survival and is the most commonly mutated oncogene in all cancers. Activating KRAS mutations are present in over 90% of pancreatic ductal adenocarcinoma (PDAC) cases and are implicated in tumor initiation and progression. Although KRAS is a critical oncogene, and therefore an important therapeutic target, its therapeutic inhibition has been very challenging, and only recently specific mutant KRAS inhibitors have been discovered. In this review, we discuss the activation of KRAS signaling and the role of mutant KRAS in PDAC development. KRAS has long been considered undruggable, and many drug discovery efforts which focused on indirect targeting have been unsuccessful. We discuss the various efforts for therapeutic targeting of KRAS. Further, we explore the reasons behind these obstacles, novel successful approaches to target mutant KRAS including G12C mutation as well as the mechanisms of resistance.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsPharmaceutical PreparationsCell ProliferationHumansMutationProto-Oncogene Proteins p21(ras)KRAS protein, humanPharmaceutical PreparationsProto-Oncogene Proteins p21(ras)KRASKRASG12CKRASG12C inhibitorsKRAS inhibitorKRAS vaccinePancreatic cancerPROTACs

Identifiers

PMID34499267
PMCPMC8556325
OpenAlexW3198590238

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.