Evidence map›Paper›PMID 21737505›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2011

Targeting SRC in mucinous ovarian carcinoma.

Koji Matsuo, Masato Nishimura, Justin N Bottsford-Miller, Jie Huang, Kakajan Komurov, Guillermo N Armaiz-Pena, Mian M K Shahzad, Rebecca L Stone, Ju Won Roh, Angela M Sanguino and 14 more

Expression of concernOpen access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It carries an expression of concern. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 43 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Targeted therapy for mucinous ovarian carcinoma: evidence from clinical trials.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2023
    Review
  5. Review
  6. Observational
  7. Article
  8. Molecular cancer therapeutics · 2019
    Article
  9. Observational
  10. Recent Insights into Mucinous Ovarian Carcinoma.International journal of molecular sciences · 2018
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. The promise and challenge of ovarian cancer models.Translational cancer research · 2015
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 5 institutions in 2 countries.

Koji MatsuoDepartment of Gynecologic Oncology and Reproductive Medicine, MD Anderson Cancer Center, University of Texas, 77230, USA.
Masato Nishimura
Justin N Bottsford-Miller
Jie Huang
Kakajan Komurov
Guillermo N Armaiz-Pena
Mian M K Shahzad
Rebecca L Stone
Ju Won Roh
Angela M Sanguino
Chunhua Lu
Dwight D Im
Neil B Rosenshien
Atsuko Sakakibara
Tadayoshi Nagano
Masato Yamasaki
Takayuki Enomoto
Tadashi Kimura
Prahlad T Ram
Kathleen M Schmeler
Gary E Gallick
Kwong K Wong
Michael Frumovitz
Anil K Sood
Kitano Hospital · JPUniversity of Wisconsin–Madison · USOsaka Rosai Hospital · JPOsaka University · JPTokushima University · JP

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
UNIVERSITY OF TEXAS MD ANDERSON SPORE IN OVARIAN CANCERP50CA083639 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BAST, ROBERT C · 1999 to 2015
$33.0M
Targeting the PI3K Signaling Pathway in Endometrial CarcinomaP50CA098258 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BROADDUS, RUSSELL R · 2003 to 2020
$32.0M
Training of Academic Gynecologic OncologistsT32CA101642 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ANIL K SOOD, Kathleen Schmeler · 2005 to 2026
$9.2M
Ovarian Cancer: Mechanisms of Neuroendocrine RegulationR01CA109298 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SOOD, ANIL K · 2005 to 2017
$4.5M
Subcellular localization of nanoparticlesRC2GM092599 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHIU, WAH, DECUZZI, PAOLO · 2009 to 2010
$3.0M
Tumor metastasis: Biobehavioral mechanismsR01CA110793 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SOOD, ANIL K · 2004 to 2009
$2.1M
Nanovectors for Characterization and Destruction of Breast Tumor VasculatureR01CA128797 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2007 to 2010
$1.7M
NCI NIH HHS CA110793NCI NIH HHS CA128797NCI NIH HHS CA16672NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA083639NCI NIH HHS P50 CA098258NCI NIH HHS R01 CA109298NCI NIH HHS R01 CA110793NCI NIH HHS R01 CA128797NCI NIH HHS T32 CA101642NIGMS NIH HHS RC2 GM092599NIGMS NIH HHS RC2GM092599PHS HHS 109298
6 · The paper itself

Abstract

purposeMucinous ovarian carcinomas have a distinct clinical pattern compared with other subtypes of ovarian carcinoma. Here, we evaluated (i) stage-specific clinical significance of mucinous ovarian carcinomas in a large cohort and (ii) the functional role of Src kinase in preclinical models of mucinous ovarian carcinoma. EXPERIMENTAL

designA total of 1,302 ovarian cancer patients including 122 (9.4%) cases of mucinous carcinoma were evaluated for survival analyses. Biological effects of Src kinase inhibition were tested using dasatinib-based therapy in a novel orthotopic mucinous ovarian cancer model (RMUG-S-ip2).

resultsPatients with advanced-stage mucinous ovarian cancer had significantly worse survival than those with serous histology: median overall survival, 1.67 versus 3.41 years, P = 0.002; median survival time after recurrence of 0.53 versus 1.66 years, P < 0.0001. Among multiple ovarian cancer cell lines, RMUG-S-ip2 mucinous ovarian cancer cells showed the highest Src kinase activity. Moreover, oxaliplatin treatment induced phosphorylation of Src kinase. This induced activity by oxaliplatin therapy was inhibited by concurrent administration of dasatinib. Targeting Src with dasatinib in vivo showed significant antitumor effects in the RMUG-S-ip2 model but not in the serous ovarian carcinoma (SKOV3-TR) model. Combination therapy of oxaliplatin with dasatinib further showed significant effects on reducing cell viability, increasing apoptosis, and in vivo antitumor effects in the RMUG-S-ip2 model.

conclusionsOur results suggest that poor survival of women with mucinous ovarian carcinoma is associated with resistance to cytotoxic therapy. Targeting Src kinase with a combination of dasatinib and oxaliplatin may be an attractive approach for this disease.

Indexed as

Adenocarcinoma, MucinousAdultAgedAnimalsAntineoplastic AgentsApoptosisBlotting, WesternCell Line, TumorCell SurvivalDasatinibFemaleGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateMiceMice, NudeAntineoplastic AgentsDasatinibOrganoplatinum CompoundsOxaliplatinProtein Kinase InhibitorsPyrimidinessrc-Family KinasesThiazoles

Identifiers

PMID21737505
PMCPMC4028171
OpenAlexW2096412326

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Registered trials

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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.