Evidence map›Paper›PMID 31908491›Full record

ArticleOncoTargets and therapy2019

Demethylation and Overexpression of CSF2 are Involved in Immune Response, Chemotherapy Resistance, and Poor Prognosis in Colorectal Cancer.

Zongbin Xu, Yiyi Zhang, Meifang Xu, Xin Zheng, Mengxin Lin, Jie Pan, Chengwei Ye, Yu Deng, Caiyun Jiang, Yu Lin and 2 more

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

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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

12 authors at 1 institution in 1 country.

Zongbin Xu *Department of Colorectal Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Yiyi Zhang *Department of Colorectal Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Meifang Xu *Department of Pathology, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Xin ZhengDepartment of Pathology, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Mengxin LinDepartment of Oncology, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Jie PanDepartment of Emergency Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Chengwei YeDepartment of Colorectal Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Yu DengDepartment of Colorectal Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Caiyun JiangDepartment of Colorectal Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Yu LinDepartment of Colorectal Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.ORCID 0000-0003-2456-5244
Xingrong LuDepartment of Colorectal Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Pan ChiDepartment of Colorectal Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Fujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study aimed to evaluate the role of colony-stimulating factor 2 (CSF2) in chemotherapy resistance, prognosis, and immune response and to identify its possible mechanisms underlying drug resistance.

methodsDrug-resistant cell lines were obtained by successively increasing drug concentration. RNA-Seq was performed to screen hub genes. CSF2 expression was analyzed via immunohistochemistry. Moreover, The Cancer Genome Atlas (TCGA), Tumor Immune Estimation Resource (TIMER) dataset, and R2 platform were used to explore the correlations among CSF2 expression, prognosis, and immune response.

resultsRNA-Seq indicated that microRNAs in cancer, P53 signaling pathway, and cell cycle were associated with FOLFOX chemotherapy resistance. Protein-protein interaction (PPI), molecular complex detection (MOCDE), and qRT-PCR analysis verified CSF2 as the hub gene in chemotherapy resistance. Moreover, CSF2 expression was lower in the normal tissue than in the cancerous tissue (P<0.05). Higher expression of CSF2 was associated with poor OS and DFS in colon cancer patients (P<0.05). We further found similar results in the Oncomine database and R2 platform (P<0.05). A higher expression of CSF2 in the CRC tissue may be caused by demethylation, which was verified using the TCGA datasets. Moreover, GSEA demonstrated that CSF2 was associated with immune response, which was consistent with results reported using TIMER datasets.

conclusionCSF2 is a novel biomarker and a prognostic factor for the survival of CRC patients affecting the immune response, and an overexpression of CSF2 in CRC patients may be caused by DNA demethylation.

Indexed as

colorectal cancerCSF2FOLFOXimmune responseprognosis

Identifiers

PMID31908491
PMCPMC6927609
OpenAlexW2996183398

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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.