Evidence map›Paper›PMID 26253275›Full record

ReviewCellular and molecular life sciences : CMLS2015

Functional and therapeutic significance of protein kinase D enzymes in invasive breast cancer.

Nisha Durand, Sahra Borges, Peter Storz

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Golgi Drivers of Cancer.Sub-cellular biochemistry · 2026
    Review
  2. Article
  3. Review
  4. Review
  5. Effect of protein kinase D inhibitor CRT0066101 on the cell migration of salivary adenoid cystic carcinoma.Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2022
    Article
  6. Review
  7. Review
  8. Article
  9. Regulation of cancer stem cells in triple negative breast cancer.Cancer drug resistance (Alhambra, Calif.) · 2021
    Review
  10. Review
  11. Protein kinase D up-regulates transcription ofThe Journal of biological chemistry · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  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

3 authors at 2 institutions in 1 country.

Nisha DurandDepartment of Cancer Biology, Mayo Clinic, Griffin Room 306, 4500 San Pablo Road, Jacksonville, FL, 32224, USA.
Sahra BorgesDepartment of Cancer Biology, Mayo Clinic, Griffin Room 306, 4500 San Pablo Road, Jacksonville, FL, 32224, USA.
Peter StorzDepartment of Cancer Biology, Mayo Clinic, Griffin Room 306, 4500 San Pablo Road, Jacksonville, FL, 32224, USA. storz.peter@mayo.edu.
Mayo Clinic in Florida · USMayo Clinic · US

Funding

The Role of CHFR in Tumorigenesis and Paclitaxel-Sensitivity in Breast CancerP50CA116201 · NCI · MAYO CLINIC ROCHESTER · PI PETER C LUCAS · 2005 to 2026
$49.9M
Role of Protein Kinase D in Actin Remodeling and Cell MotiliyR01GM086435 · NIGMS · MAYO CLINIC JACKSONVILLE · PI STORZ, PETER · 2010 to 2013
$1.1M
Targeting Protein Kinase D in Triple Negative Breast CancersR21CA184527 · NCI · MAYO CLINIC JACKSONVILLE · PI STORZ, PETER · 2015 to 2016
$374k
NCI NIH HHS CA116201-03DR4NCI NIH HHS CA184527NCI NIH HHS P50 CA116201NCI NIH HHS R21 CA184527NIGMS NIH HHS GM086435NIGMS NIH HHS R01 GM086435
6 · The paper itself

Abstract

The protein kinase D (PKD) family members, PKD1, PKD2 and PKD3 constitute a family of serine/threonine kinases that are essential regulators of cell migration, proliferation and protein transport. Multiple types of cancers are characterized by aberrant expression of PKD isoforms. In breast cancer PKD isoforms exhibit distinct expression patterns and regulate various oncogenic processes. In highly invasive breast cancer, the leading cause of cancer-associated deaths in females, the loss of PKD1 is thought to promote invasion and metastasis, while PKD2 and upregulated PKD3 have been shown to be positive regulators of proliferation, chemoresistance and metastasis. In this review, we examine the differential expression pattern, mechanisms of regulation and contributions made by each PKD isoform to the development and maintenance of invasive breast cancer. In addition, we discuss the potential therapeutic approaches for targeting PKD in this disease.

Indexed as

Breast NeoplasmsCell MovementCell ProliferationFemaleHumansIsoenzymesModels, BiologicalNeoplasm InvasivenessProtein Kinase CProtein Kinase InhibitorsIsoenzymesProtein Kinase Cprotein kinase DProtein Kinase InhibitorsInvasionInvasive breast cancerMulti-drug resistancePKDProtein kinase D

Identifiers

PMID26253275
PMCPMC4618102
OpenAlexW1072204632

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.