Evidence map›Paper›PMID 26206252›Full record

ReviewJournal of cellular biochemistry2016

Control of Apoptosis in Treatment and Biology of Pancreatic Cancer.

Shrey Modi, Devika Kir, Sulagna Banerjee, Ashok Saluja

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Journal of cellular biochemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06387342 (CF102-222PC), which is not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
0.6field-weighted citation impact, top 31% 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.

NCT06387342 phase2recruitingnot on this mapstarted 2024, after this paper: background citation

CF102-222PC: A Phase 2 Open-Label Study of the Safety and Activity of Namodenoson in the Treatment of Advanced Pancreatic Adenocarcinoma

TypeinterventionalSponsorCan-Fite BioPharmaRan2024 to 2026Enrolled20ConditionsPancreatic Adenocarcinoma, Pancreatic CancerArmsNamodenoson 25mg
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 50 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Recent advances in drug delivery and targeting for the treatment of pancreatic cancer.Journal of controlled release : official journal of the Controlled Release Society · 2024
    Review
  7. Article
  8. Review
  9. Necroptosis activation is associated with greater methylene blue-photodynamic therapy-induced cytotoxicity in human pancreatic ductal adenocarcinoma cells.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2023
    Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Cell death in pancreatic cancer: from pathogenesis to therapy.Nature reviews. Gastroenterology & hepatology · 2021
    Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Shrey ModiDivision of Basic and Translational Research, Department of Surgery, Minneapolis, Minnesota.
Devika KirDivision of Basic and Translational Research, Department of Surgery, Minneapolis, Minnesota.
Sulagna BanerjeeDivision of Basic and Translational Research, Department of Surgery, Minneapolis, Minnesota.
Ashok SalujaDivision of Basic and Translational Research, Department of Surgery, Minneapolis, Minnesota.
Midwest Orthopaedic Research Foundation · US

Funding

The Inhibition of HSP70 Induces Apoptosis in Pancreatic Cancer CellsR01CA124723 · NCI · UNIVERSITY OF MINNESOTA · PI GILBOA, ELI, RAMAKRISHNAN, SUNDARAM · 2007 to 2022
$4.5M
Triptolide Augments Death Receptor Mediated Apoptosis in Pancreatic CancerR01CA170946 · NCI · UNIVERSITY OF MINNESOTA · PI SALUJA, ASHOK K · 2012 to 2016
$2.4M
Functional Significance of CD133 in Pancreatic CancerR01CA184274 · NCI · UNIVERSITY OF MINNESOTA · PI BANERJEE, SULAGNA · 2014 to 2018
$1.6M
NCI NIH HHS CA124723NCI NIH HHS R01 CA124723NCI NIH HHS R01 CA170946NCI NIH HHS R01-CA170946NCI NIH HHS R01 CA184274NCI NIH HHS R01-CA184274
6 · The paper itself

Abstract

Pancreatic cancer is estimated to be the 12th most common cancer in the United States in 2014 and yet this malignancy is the fourth leading cause of cancer-related death in the United States. Late detection and resistance to therapy are the major causes for its dismal prognosis. Apoptosis is an actively orchestrated cell death mechanism that serves to maintain tissue homoeostasis. Cancer develops from normal cells by accruing significant changes through one or more mechanisms, leading to DNA damage and mutations, which in a normal cell would induce this programmed cell death pathway. As a result, evasion of apoptosis is one of the hallmarks of cancer cells. PDAC is notoriously resistant to apoptosis, thereby explaining its aggressive nature and resistance to conventional treatment modalities. The current review is focus on understanding different intrinsic and extrinsic pathways in pancreatic cancer that may affect apoptosis in this disease.

Indexed as

ApoptosisAnimalsAntineoplastic AgentsApoptosis Regulatory ProteinsCarcinoma, Pancreatic DuctalHumansMolecular Targeted TherapyPancreatic NeoplasmsAntineoplastic AgentsApoptosis Regulatory ProteinsAPOPTOSISPANCREATIC CANCERSIGNALLINGTHERAPY

Identifiers

PMID26206252
PMCPMC5724757
OpenAlexW1822477452

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.