Evidence map›Paper›PMID 26617702›Full record

ArticleInternational journal of clinical and experimental pathology2015

Expression of Robo protein in bladder cancer tissues and its effect on the growth of cancer cells by blocking Robo protein.

Yang Li, Hepeng Cheng, Weibo Xu, Xin Tian, Xiaodong Li, Chaoyang Zhu

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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
  2. Review
  3. Identifying and treating ROBO1The Prostate · 2020
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Deep Sequencing of Urinary RNAs for Bladder Cancer Molecular Diagnostics.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Article
  9. Article
  10. Review
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 1 institution in 1 country.

Yang LiDepartment of Urology, Henan University Huaihe Hospital Kaifeng 475000, China.
Hepeng ChengDepartment of Urology, Henan University Huaihe Hospital Kaifeng 475000, China.
Weibo XuDepartment of Urology, Henan University Huaihe Hospital Kaifeng 475000, China.
Xin TianDepartment of Urology, Henan University Huaihe Hospital Kaifeng 475000, China.
Xiaodong LiDepartment of Urology, Henan University Huaihe Hospital Kaifeng 475000, China.
Chaoyang ZhuDepartment of Urology, Henan University Huaihe Hospital Kaifeng 475000, China.
Henan University Huaihe Hospital and Huaihe Clinical Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to detect the expression of Slit signaling protein ligand Robo protein in human bladder cancer and para-carcinoma tissue, and observe the tumor cell survival and growth by inoculating the bladder cancer cells with the blocked signaling protein into the subcutaneous tissue of nude mice. The expression of Robo protein was detected in T24 cells in human bladder uroepithelium carcinoma and cultivated human bladder uroepithelium carcinoma confirmed by pathological diagnosis. The cultivated T24 cells were coated by the protein antibody and human bladder uroepithelium carcinoma T24 tumor-bearing mice model was established. The tumor cell survival and growth were observed in the antibody coating group and non-coating group. The tumor body size was measured. The immunohistochemical detection showed that Robo protein isoforms Robo1 and Robo 4 were expressed in T24 cells of cancer tissues, paracarcinoma tissues and cultured human uroepithelium carcinoma. The expression of Robo1 was significantly higher than that of Robo4 (P<0.05). The cancer cells could be detected in nodular tumor of mice in each group. The volume of the tumor-bearing mice in the nodular tumor of the non-coating group was larger than that of anti-Robol antibody coating group and the difference was statistically significant (P<0.01). There was no significant difference in tumor volume between anti-Robo4 antibody coating group and non-coating group (P>0.05); The difference was statistically significant compared with the anti-Robo1 antibody coating group (P<0.01). In conclusion, Robo protein isoforms Robo1 and Robo4 were expressed in human bladder cancer T24 cells. To block Robo4 signal protein had little effect on the survival and growth of the transplantation tumor and to block Robo1 signal protein would seriously affect the survival and growth of the transplantation tumor, suggesting that Robo1 might play an important role in the growth and metastasis of bladder cancer, and might become a new target for the treatment of human bladder cancer and drug research.

Indexed as

AnimalsCarcinoma, Transitional CellCell ProliferationFemaleFluorescent Antibody TechniqueHeterograftsHumansImmunohistochemistryMaleMiceMice, Inbred BALB CMice, NudeNerve Tissue ProteinsProtein IsoformsReceptors, ImmunologicRoundabout ProteinsNerve Tissue ProteinsProtein IsoformsReceptors, ImmunologicRoundabout ProteinsBladder cancerSlit/Robo signaling pathwayT24 cells

Identifiers

PMID26617702
PMCPMC4637787
OpenAlexW2410201430

What OpenQuestion holds

Textmetadata
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.