Evidence map›Paper›PMID 20621068›Full record

ReviewBiochemical pharmacology2010

Role of protein kinase D signaling in pancreatic cancer.

Sushovan Guha, Suebpong Tanasanvimon, James Sinnett-Smith, Enrique Rozengurt

Open access · greenAbstract readReview
In one paragraph

Review in Biochemical pharmacology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

46 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. [Role of protein kinase D1 in regulating the growth, apoptosis and drug sensitivity of oral squamous carcinoma cells].Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Protein kinase D signaling in cancer: A friend or foe?Biochimica et biophysica acta. Reviews on cancer · 2017
    Review
  16. Article
  17. Role of Notch signaling pathway in pancreatic cancer.American journal of cancer research · 2017
    Review
  18. Article
  19. PKD signaling and pancreatitis.Journal of gastroenterology · 2016
    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 2 institutions in 1 country.

Sushovan GuhaDepartment of Gastroenetrology, Hepatology, and Nutrition, the UT MD Anderson Cancer Center, Unit 1466, 1515 Holcombe Boulevard, Houston, TX 77030, USA. sguha@mdanderson.org
Suebpong Tanasanvimon
James Sinnett-Smith
Enrique Rozengurt
The University of Texas MD Anderson Cancer Center · USUniversity of California, Los Angeles · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
GASTROINTESTINAL PEPTIDE SIGNALING THROUGH PKC/PKDR01DK055003 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1999 to 2011
$4.9M
GI PEPTIDE SIGNALING THROUGH TYROSINE PHOSPHORYLATIONR01DK056930 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 2000 to 2010
$3.0M
Targeting crosstalk between insulin and Gq signaling systems in pancreatic cancerR21CA137292 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 2009 to 2010
$373k
Biological and Therapeutic Significance of TG2 in Pancreatic CancerR21CA135218 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MEHTA, KAPIL · 2009 to 2010
$372k
NCI NIH HHS 5P30CA16672NCI NIH HHS P30 CA016672NCI NIH HHS R21 CA135218NCI NIH HHS R21CA135218NCI NIH HHS R21 CA137292NCI NIH HHS R21CA137292NIDDK NIH HHS P30 DK041301NIDDK NIH HHS P30DK41301NIDDK NIH HHS R01 DK055003NIDDK NIH HHS R01 DK056930NIDDK NIH HHS R01DK55003NIDDK NIH HHS R01DK56930
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal cancers with dismal survival rates. Its intransigence to conventional therapy renders PDAC an aggressive disease with early metastatic potential. Thus, novel targets for PDAC therapy are urgently needed. Multiple signal transduction pathways are implicated in progression of PDAC. These pathways stimulate production of intracellular messengers in their target cells to modify their behavior, including the lipid-derived diacylglycerol (DAG). One of the prominent intracellular targets of DAG is the protein kinase C (PKC) family. However, the mechanisms by which PKC-mediated signals are decoded by the cell remain incompletely understood. Protein kinase D1 (PKD or PKD1, initially called atypical PKCμ), is the founding member of a novel protein kinase family that includes two additional protein kinases that share extensive overall homology with PKD, termed PKD2, and PKD3. The PKD family occupies a unique position in the signal transduction pathways initiated by DAG and PKC. PKD lies downstream of PKCs in a novel signal transduction pathway implicated in the regulation of multiple fundamental biological processes. We and others have shown that PKD-mediated signaling pathways promote mitogenesis and angiogenesis in PDAC. Our recent observations demonstrate that PKD also potentiates chemoresistance and invasive potential of PDAC cells. This review will briefly highlight diverse biological roles of PKD family in multiple neoplasias including PDAC. Further, this review will underscore our latest advancement with the development of a potent PKD family inhibitor and its effect both in vitro and in vivo in PDAC.

Indexed as

AnimalsAntineoplastic AgentsCarcinoma, Pancreatic DuctalCell MovementCell PolarityCell ProliferationEpithelial CellsHeat-Shock ProteinsHumansInflammationMolecular Targeted TherapyNeovascularization, PathologicOxidative StressPancreatic NeoplasmsProtein Kinase CProtein Kinase D2Antineoplastic AgentsHeat-Shock ProteinsProtein Kinase Cprotein kinase C nuprotein kinase DProtein Kinase D2Protein Kinases

Identifiers

PMID20621068
PMCPMC2974013
OpenAlexW2001179486

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.