Evidence map›Paper›PMID 29844821›Full record

ArticleOncology letters2018

Tumor-derived mesenchymal-stem-cell-secreted IL-6 enhances resistance to cisplatin via the STAT3 pathway in breast cancer.

Huitao Xu, Ying Zhou, Wei Li, Bin Zhang, Huanhuan Zhang, Shaolin Zhao, Ping Zheng, Huiyi Wu, Jin Yang

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

30 citing papers in PubMed, 51 citations in OpenAlex.

  1. Hyptolide Promotes Breast Cancer Stem Cells Apoptosis and S-phase Cell Cycle Arrest.Asian Pacific journal of cancer prevention : APJCP · 2025
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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

9 authors at 2 institutions in 1 country.

Huitao XuDepartment of Central Laboratory, The First People's Hospital of Lianyungang, Lianyungang, Jiangsu 222002, P.R. China.
Ying ZhouDepartment of Central Laboratory, The First People's Hospital of Lianyungang, Lianyungang, Jiangsu 222002, P.R. China.
Wei LiDepartment of Central Laboratory, The First People's Hospital of Lianyungang, Lianyungang, Jiangsu 222002, P.R. China.
Bin ZhangSchool of Medical Science and Laboratory Medicine, Jiangsu University, Zhenjiang, Jiangsu 212000, P.R. China.
Huanhuan ZhangDepartment of Central Laboratory, The First People's Hospital of Lianyungang, Lianyungang, Jiangsu 222002, P.R. China.
Shaolin ZhaoDepartment of Central Laboratory, The First People's Hospital of Lianyungang, Lianyungang, Jiangsu 222002, P.R. China.
Ping ZhengDepartment of Central Laboratory, The First People's Hospital of Lianyungang, Lianyungang, Jiangsu 222002, P.R. China.
Huiyi WuDepartment of Central Laboratory, The First People's Hospital of Lianyungang, Lianyungang, Jiangsu 222002, P.R. China.
Jin YangDepartment of Central Laboratory, The First People's Hospital of Lianyungang, Lianyungang, Jiangsu 222002, P.R. China.
The First People’s Hospital of Lianyungang · CNJiangsu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cisplatin is used for the treatment of a range of solid malignant tumors; however, with prolonged treatment durations, the sensitivity of tumor cells to the drug decreases owing to an unclear mechanism of drug resistance. The present study aimed to investigate whether breast-cancer-tissue-derived mesenchymal stem cells (BC-MSCs) are involved in mediating the effects of cisplatin on breast cancer cells, and which component of the BC-MSC conditioned medium (BC-MSC-CM) exhibited an anti-apoptotic effect. Cytokines/chemokines in BC-MSC-CM were quantified using a Luminex immunoassay, and reverse transcription-quantitative polymerase chain reaction analysis detected interleukin-6 (IL-6) levels in MCF-7 cells following different treatments. MTT and flow cytometry analysis measured cell vitality and apoptosis, respectively, and activation of signal transduced and activator of transcription 3 (STAT3) was evaluated by western blotting. BC-MSCs reversed the pro-apoptotic effect of cisplatin and enhanced the proliferation of MCF-7 cells more potently than bone-marrow-derived MSCs. Further study revealed that BC-MSCs secreted IL-6 to protect MCF-7 cells from apoptosis and promote their survival. Neutralizing IL-6 with a specific antibody partially inhibited the IL-6/STAT3 signaling pathway and reversed the promoter role of BC-MSCs in MCF-7 cells. Taken together, the findings of the present study indicated that BC-MSCs decreased the level of cisplatin-induced apoptosis in MCF-7 cells by activating the IL-6/STAT3 pathway in cancer cells. BC-MSCs, as important cells in the tumor microenvironment, have a key role in the treatment of breast cancer.

Indexed as

apoptosisbreast cancerbreast-cancer-derived mesenchymal stem cellscisplatininterleukin-6tumor microenvironment

Identifiers

PMID29844821
PMCPMC5958889
OpenAlexW2797287370

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.