Evidence map›Paper›PMID 31970165›Full record

ArticleWorld journal of clinical cases2020

Oncogenic role of Tc17 cells in cervical cancer development.

Zun-Sheng Zhang, Ying Gu, Bing-Gang Liu, Hong Tang, Yu Hua, Jun Wang

Open access · diamondAbstract read
In one paragraph

Article in World journal of clinical cases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Cervical Cancer Immunotherapy: Facts and Hopes.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    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.

Zun-Sheng ZhangDepartment of Obstetrics and Gynecology, Shanghai Seventh People's Hospital, Shanghai 200120, China.
Ying GuDepartment of Obstetrics and Gynecology, Shanghai Seventh People's Hospital, Shanghai 200120, China.
Bing-Gang LiuDepartment of Obstetrics and Gynecology, Shanghai Seventh People's Hospital, Shanghai 200120, China.
Hong TangDepartment of Obstetrics and Gynecology, Shanghai Seventh People's Hospital, Shanghai 200120, China.
Yu HuaDepartment of Obstetrics and Gynecology, Shanghai Seventh People's Hospital, Shanghai 200120, China.
Jun WangDepartment of Obstetrics and Gynecology, Shanghai Seventh People's Hospital, Shanghai 200120, China. wanchuang3069629@163.com.
Seventh People's Hospital of Shanghai · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs one of the subsets of CD8

aimTo assess the status of Tc17 cells in cervical cancer and investigate the biological function of Tc17 cells in cervical cancer development.

methodsFlow cytometry assay, immunohistochemistry, and immunofluorescence were performed to detect the levels and phenotype of Tc17 cells in blood and tumor samples from patients with cervical cancer. Prior to cell suspension culture, ELISA was carried out to measure the production of IL-6, IL-1β, IL-23, CXCL12, and IL-17 in tumor tissue supernatant and co-cultured supernatant of patients with cervical cancer. In addition, multivariate analysis was performed to identify factors associated with overall survival using the Cox proportional hazards model.

resultsCompared with normal tissues, Tc17 cells specifically accumulated in tumor tissues of cervical cancer patients. Cancer cells produced a greater amount of IL-6, IL-1β, and IL-23, which in turn promoted Tc17 cell polarization. Unlike the traditional cytotoxic CD8

conclusionOur data identified the oncogenic role of Tc17 cells in the development of cervical cancer. We propose that the ratio of Tc17 cells may be a useful index in the prognosis of patients with cervical cancer.

Indexed as

Biological functionCancer developmentCervical cancerInterleukin-17Oncogenic roleTc17 cells

Identifiers

PMID31970165
PMCPMC6962079
OpenAlexW2997131473

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.