Evidence map›Paper›PMID 30066897›Full record

ArticleOncology reports2018

Dowregulation of OTX1 attenuates gastric cancer cell proliferation, migration and invasion.

Shi-Chen Qin, Zhong Zhao, Jin-Xin Sheng, Xiang-Hui Xu, Jie Yao, Jin-Jun Lu, Bin Chen, Guo-Dong Zhao, Xiao-Yong Wang, Yan-Dong Yang

Open access · hybridAbstract read
In one paragraph

Article in Oncology reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  3. International journal of molecular sciences · 2023
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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

10 authors.

Shi-Chen QinDepartment of General Surgery, Haimen People's Hospital, Haimen, Jiangsu 226100, P.R. China.
Zhong ZhaoDepartment of General Surgery, Haimen People's Hospital, Haimen, Jiangsu 226100, P.R. China.
Jin-Xin ShengDepartment of General Surgery, Haimen People's Hospital, Haimen, Jiangsu 226100, P.R. China.
Xiang-Hui XuDepartment of General Surgery, Haimen People's Hospital, Haimen, Jiangsu 226100, P.R. China.
Jie YaoDepartment of General Surgery, Haimen People's Hospital, Haimen, Jiangsu 226100, P.R. China.
Jin-Jun LuDepartment of General Surgery, Haimen People's Hospital, Haimen, Jiangsu 226100, P.R. China.
Bin ChenDepartment of General Surgery, Haimen People's Hospital, Haimen, Jiangsu 226100, P.R. China.
Guo-Dong ZhaoDepartment of General Surgery, Haimen People's Hospital, Haimen, Jiangsu 226100, P.R. China.
Xiao-Yong WangDepartment of General Surgery, Haimen People's Hospital, Haimen, Jiangsu 226100, P.R. China.
Yan-Dong YangDepartment of General Surgery, Haimen People's Hospital, Haimen, Jiangsu 226100, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Orthodenticle homolog 1 (OTX1) has previously been revealed to be tightly associated with the development and progression of several human tumors. However, the functional roles and underlying molecular mechanisms of OTX1 in gastric cancer (GC) remain poorly understood. In the present study, we observed that OTX1 was highly expressed in GC tissues compared with adjacent non‑tumor tissues based on a large cohort of samples from The Cancer Genome Atlas (TCGA) database. An immunohistochemical analysis indicated that OTX1 levels were increased in tumors that became metastatic compared with those in tumors that did not. This finding was significantly associated with patients who had shorter overall survival times. The knockdown of OTX1 significantly inhibited the proliferation, migration and invasion of SGC‑7901 and MGC‑803 cells. Furthermore, the knockdown of OTX1 induced cell cycle arrest in the G0/G1 phase and reduced the expression of cyclin D1. In addition, the inhibition of OTX1 led to increased GC cell apoptosis by upregulating cleaved PARP, cleaved caspase‑3 and Bax. In conclusion, our data indicated that OTX1 functions as a key regulator in tumor growth and metastasis of GC cells. Thus, OTX1 may be a promising novel target for molecular therapy directed toward GC.

Indexed as

Cell MovementCell ProliferationAdultAgedAged, 80 and overApoptosisBiomarkers, TumorCase-Control StudiesFemaleFollow-Up StudiesGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNeoplasm InvasivenessOtx Transcription FactorsBiomarkers, TumorOTX1 protein, humanOtx Transcription Factors

Identifiers

PMID30066897
PMCPMC6111461
OpenAlexW2883848251

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.