Evidence map›Paper›PMID 26725045›Full record

ReviewArchivum immunologiae et therapiae experimentalis2016

Novel Insights into the Roles of Rho Kinase in Cancer.

Lei Wei, Michelle Surma, Stephanie Shi, Nathan Lambert-Cheatham, Jianjian Shi

Registry-linked trialOpen access · hybridAbstract readReview
In one paragraph

Review in Archivum immunologiae et therapiae experimentalis, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06890858 (A Clinical Study on Fasudil Hydrochloride for Treatment of Gene-Specific Ovarian Cancer), which is not on this map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
12.9field-weighted citation impact, top 1% 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.

NCT06890858 phase2recruitingnot on this mapstarted 2025, after this paper: background citation

A Clinical Study on Fasudil Hydrochloride for Treatment of Gene-Specific Ovarian Cancer

TypeinterventionalSponsorZhejiang Provincial People's HospitalRan2025 to 2028Enrolled20ConditionsOvarian CancerArmsFasudil Hydrochloride
3 · Its place in the literature

Who cites it

104 citing papers in PubMed, 200 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Rho/ROCK Pathway as a Therapeutic Target in Multiple Diseases.International journal of drug discovery and pharmacology · 2025
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article

44 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

5 authors at 2 institutions in 1 country.

Lei WeiRiley Heart Research Center, Herman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University, School of Medicine, R4 Building, Room 332, 1044 West Walnut Street, Indianapolis, IN, 46202-5225, USA. lewei@iu.edu.
Michelle SurmaRiley Heart Research Center, Herman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University, School of Medicine, R4 Building, Room 332, 1044 West Walnut Street, Indianapolis, IN, 46202-5225, USA.
Stephanie ShiRiley Heart Research Center, Herman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University, School of Medicine, R4 Building, Room 332, 1044 West Walnut Street, Indianapolis, IN, 46202-5225, USA.
Nathan Lambert-CheathamRiley Heart Research Center, Herman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University, School of Medicine, R4 Building, Room 332, 1044 West Walnut Street, Indianapolis, IN, 46202-5225, USA.
Jianjian ShiRiley Heart Research Center, Herman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University, School of Medicine, R4 Building, Room 332, 1044 West Walnut Street, Indianapolis, IN, 46202-5225, USA. jishi@iu.edu.
Indiana University – Purdue University Indianapolis · USIndiana University School of Medicine

Funding

Regulation of cardiac stress responses by Rho kinaseR01HL107537 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI WEI, LEI · 2013 to 2016
$1.5M
NHLBI NIH HHS R01 HL107537
6 · The paper itself

Abstract

Rho-associated coiled-coil kinase (ROCK) is a major downstream effector of the small GTPase RhoA. The ROCK family, consisting of ROCK1 and ROCK2, plays a central role in the organization of the actin cytoskeleton, and is involved in a wide range of fundamental cellular functions such as contraction, adhesion, migration, proliferation, and apoptosis. Since the discovery of effective inhibitors such as fasudil and Y27632, the biological roles of ROCK have been extensively explored in numerous diseases, including cancer. Accumulating evidence supports the concept that ROCK plays important roles in tumor development and progression through regulating many key cellular functions associated with malignancy, including tumorigenicity, tumor growth, metastasis, angiogenesis, tumor cell apoptosis/survival and chemoresistance as well. This review focuses on the new advances of the most recent 5 years from the studies on the roles of ROCK in cancer development and progression; the discussion is mainly focused on the potential value of ROCK inhibitors in cancer therapy.

Indexed as

ApoptosisCell AdhesionCell MovementCell ProliferationCell SurvivalDisease ProgressionDrug Resistance, NeoplasmHumansMicroRNAsMutationNeoplasm MetastasisNeoplasmsNeoplastic Stem CellsNeovascularization, PathologicPolymorphism, GeneticProtein IsoformsMicroRNAsProtein Isoformsrho-Associated KinasesROCK1 protein, humanROCK2 protein, humanCancer therapyRho kinaseRho kinase pan-inhibitorROCK isoform-specific inhibitor

Identifiers

PMID26725045
PMCPMC4930737
OpenAlexW2215155470

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.