Evidence map›Paper›PMID 31933924›Full record

ArticleInternational journal of clinical and experimental pathology2019

SREBP1 promotes 5-FU resistance in colorectal cancer cells by inhibiting the expression of caspase7.

Yuyan Gao, Qi Zhao, Xiaoqin Mu, Huifen Zhu, Binbin Liu, Bingqing Yao, Xinyi Liu, Wenhan Xue, Bo Wang, Shulin Liu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

8 citing papers in PubMed, 17 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

10 authors at 1 institution in 1 country.

Yuyan GaoDepartment of Radiotherapy, Beijing Luhe Hospital, Affiliated to Capital Medical University Beijing, China.
Qi ZhaoDepartment of Gastrointestinal Medical Oncology, The Affiliated Tumor Hospital of Harbin Medical University Harbin, China.
Xiaoqin MuSystemomics Center, College of Pharmacy, Genomics Research Center, Harbin Medical University Harbin, China.
Huifen ZhuSystemomics Center, College of Pharmacy, Genomics Research Center, Harbin Medical University Harbin, China.
Binbin LiuSystemomics Center, College of Pharmacy, Genomics Research Center, Harbin Medical University Harbin, China.
Bingqing YaoSystemomics Center, College of Pharmacy, Genomics Research Center, Harbin Medical University Harbin, China.
Xinyi LiuSystemomics Center, College of Pharmacy, Genomics Research Center, Harbin Medical University Harbin, China.
Wenhan XueSystemomics Center, College of Pharmacy, Genomics Research Center, Harbin Medical University Harbin, China.
Bo WangSystemomics Center, College of Pharmacy, Genomics Research Center, Harbin Medical University Harbin, China.
Shulin LiuSystemomics Center, College of Pharmacy, Genomics Research Center, Harbin Medical University Harbin, China.
Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe role of lipid metabolism played in cancer cell growth attracts more attention. SREBP1 is a common lipid regulatory factor. It has been reported that SREBP1 can promote tumor cell resistance. The aim of this study was to investigate its role in chemoresistance of colorectal cancer (CRC).

methodsThe expression of SREBP1 in CRC tissues was analyzed by immunohistochemistry. Using a viability assay, the sensitivity to 5-fluorouracil in two colon cancer cell lines (HT-29 and SW620) was measured and its correlation with different expression levels of SREBP1 protein by western blot was investigated.

resultsThe protein expression of SREBP1 in CRC tissues was higher than that in normal colon tissues. We found that over-expression of SREBP1 through SREBP1 gene transfection enhances the resistant of CRC cell lines to 5-FU, and SREBP1 silencing through SREBP1 shRNA transfection can promote apoptosis in 5-FU treated SW620 cells. Further study indicated that SREBP1 could inhibit the expression of caspase7 and reduce PARP1 cleavage fragments.

conclusionOur results suggest that SREBP1 protect the 5-FU treated CRC cells through caspase7 dependent PARP1 cleavage in apoptosis pathway and potentially provide a new target in the treatment of CRC.

Indexed as

caspase7Colorectal cancer (CRC)resistancesterol-regulatory element binding protein 1 (SREBP1)

Identifiers

PMID31933924
PMCPMC6945170
OpenAlexW3007088667

What OpenQuestion holds

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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.