Evidence map›Paper›PMID 26617739›Full record

ArticleInternational journal of clinical and experimental pathology2015

Elevated expression of RIT1 correlates with poor prognosis in endometrial cancer.

Fengjuan Xu, Su'an Sun, Shilan Yan, Hongling Guo, Miao Dai, Yincheng Teng

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
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  12. Review
  13. Genomic Landscape of Uterine Sarcomas Defined Through Prospective Clinical Sequencing.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Observational
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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

6 authors at 3 institutions in 1 country.

Fengjuan XuDepartment of Obstetrics and Gynecology, The First People's Hospital of Taicang Jiangsu, PR China.
Su'an SunDepartment of Obstetrics and Gynecology, Huai'an First People's Hospital, Nanjing Medical University Huai'an, Jiangsu, PR China.
Shilan YanDepartment of Obstetrics and Gynecology, Huai'an First People's Hospital, Nanjing Medical University Huai'an, Jiangsu, PR China.
Hongling GuoDepartment of Obstetrics and Gynecology, The First People's Hospital of Taicang Jiangsu, PR China.
Miao DaiDepartment of Obstetric and Gynecology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital Shanghai, PR China.
Yincheng TengDepartment of Obstetric and Gynecology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital Shanghai, PR China.
Huaian First People’s Hospital · CNShanghai Sixth People's Hospital · CNTaizhou First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RIT1, (Ras-like without CAAX1), the founding member of a novel branch of the Ras subfamily, mediates a wide variety of cellular functions, including cell proliferation, survival, and differentiation, and it may play crucial oncogenic role in human cancer. The purpose of the current study was to characterize the expression pattern of RIT1 and assess the clinical significance of RIT1 expression in endometrial cancer patients. The mRNA and protein expression of RIT1 was significantly overexpressed in 7 endometrial cancer cell lines by qPCR and Western blot, respectively. In addition, RIT1 mRNA expression was elevated in 36 freshly frozen endometrial cancer tissues compared to 21 non-cancerous endometrial tissue samples. Similar results were observed by analyzing GEO datasets. Immunohistochemistry was used to examine the protein expression of RIT1 in two tissue microarrays containing 257 cases of tumor and 31 non-tumor tissues, which showed that elevated expression of RIT1 was significantly correlated with pathological type, clinical stage, grade and vascular invasion. Importantly, Kaplan-Meier survival analysis indicated that RIT1 expression was associated with overall survival of endometrial cancer patients. Multivariate Cox regression analysis revealed that RIT1 expression was one of the independent prognostic factors for endometrial cancer patients. Furthermore, RIT1 combined with other clinicopathological risk factors was a more significant model in ROC curve comparison. In conclusion, elevated expression of RIT1 may contribute to the progression of endometrial cancer and thus may serve as a novel prognostic marker and a promising molecular target for the treatment of endometrial cancer.

Indexed as

AdultCarcinomaCell DifferentiationCell Line, TumorCell ProliferationCell SurvivalDisease ProgressionEndometrial NeoplasmsFemaleHumansMiddle AgedNeoplasm StagingPrognosisras ProteinsSurvival Rateras ProteinsRIT1 protein, humanendometrial cancerpoor prognosisRIT1

Identifiers

PMID26617739
PMCPMC4637554
OpenAlexW2417380023

What OpenQuestion holds

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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.