Evidence map›Paper›PMID 36765737›Full record

ReviewCancers2023

Genetics, Genomics and Emerging Molecular Therapies of Pancreatic Cancer.

Jakub Liu, Magdalena Mroczek, Anna Mach, Maria Stępień, Angelika Aplas, Bartosz Pronobis-Szczylik, Szymon Bukowski, Magda Mielczarek, Ewelina Gajewska, Piotr Topolski and 3 more

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Causal Exposures in Pancreatic Cancer Incidence: Insights From Mendelian Randomization Studies.JGH open : an open access journal of gastroenterology and hepatology · 2025
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. 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

13 authors at 5 institutions in 2 countries.

Jakub LiuBiostatistics Group, Wroclaw University of Environmental and Life Sciences, 51-631 Wroclaw, Poland.
Magdalena MroczekCentre for Cardiovascular Genetics and Gene Diagnostics, Foundation for People with Rare Diseases, Wagistrasse 25, 8952 Schlieren, Switzerland.ORCID 0000-0002-8731-0540
Anna MachDepartment of Psychiatry, Medical University of Warsaw, 00-665 Warsaw, Poland.
Maria StępieńDepartment of Infectious Diseases, Doctoral School, Medical University of Lublin, 20-059 Lublin, Poland.ORCID 0000-0002-3377-4665
Angelika AplasCentral Clinical Hospital of Ministry of the Interior and Administration in Warsaw, 02-507 Warsaw, Poland.
Bartosz Pronobis-SzczylikCentral Clinical Hospital of Ministry of the Interior and Administration in Warsaw, 02-507 Warsaw, Poland.
Szymon BukowskiCentral Clinical Hospital of Ministry of the Interior and Administration in Warsaw, 02-507 Warsaw, Poland.
Magda MielczarekBiostatistics Group, Wroclaw University of Environmental and Life Sciences, 51-631 Wroclaw, Poland.ORCID 0000-0002-1086-9119
Ewelina GajewskaCentral Clinical Hospital of Ministry of the Interior and Administration in Warsaw, 02-507 Warsaw, Poland.
Piotr TopolskiCentral Clinical Hospital of Ministry of the Interior and Administration in Warsaw, 02-507 Warsaw, Poland.
Zbigniew J KrólCentral Clinical Hospital of Ministry of the Interior and Administration in Warsaw, 02-507 Warsaw, Poland.ORCID 0000-0003-3162-8813
Joanna SzydaBiostatistics Group, Wroclaw University of Environmental and Life Sciences, 51-631 Wroclaw, Poland.ORCID 0000-0001-9688-0193
Paula DoboszCentral Clinical Hospital of Ministry of the Interior and Administration in Warsaw, 02-507 Warsaw, Poland.
Central Clinical Hospital · PLWrocław University of Environmental and Life Sciences · PLFoundation for People with Rare Diseases · CHMedical University of Lublin · PLMedical University of Warsaw · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The number of cases of pancreatic cancers in 2019 in Poland was 3852 (approx. 2% of all cancers). The course of the disease is very fast, and the average survival time from the diagnosis is 6 months. Only <2% of patients live for 5 years from the diagnosis, 8% live for 2 years, and almost half live for only about 3 months. A family predisposition to pancreatic cancer occurs in about 10% of cases. Several oncogenes in which somatic changes lead to the development of tumours, including genes BRCA1/2 and PALB2, TP53, CDKN2A, SMAD4, MLL3, TGFBR2, ARID1A and SF3B1, are involved in pancreatic cancer. Between 4% and 10% of individuals with pancreatic cancer will have a mutation in one of these genes. Six percent of patients with pancreatic cancer have NTRK pathogenic fusion. The pathogenesis of pancreatic cancer can in many cases be characterised by homologous recombination deficiency (HRD)-cell inability to effectively repair DNA. It is estimated that from 24% to as many as 44% of pancreatic cancers show HRD. The most common cause of HRD are inactivating mutations in the genes regulating this DNA repair system, mainly BRCA1 and BRCA2, but also PALB2, RAD51C and several dozen others.

Indexed as

geneticsgenomicsmolecular therapiespancreatic cancer

Identifiers

PMID36765737
PMCPMC9913594
OpenAlexW4318485090

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.