Evidence map›Paper›PMID 27034162›Full record

ArticleOncotarget2016

FOXM1 promotes invasion and migration of colorectal cancer cells partially dependent on HSPA5 transactivation.

Xiaoyong Luo, Jinke Yao, Peipei Nie, Zhiyuan Yang, Hongbo Feng, Pinjia Chen, Xinpeng Shi, Zhengzhi Zou

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
4.4field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 2 syntheses or guidelines pooled it, 48 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

8 authors at 3 institutions in 1 country.

Xiaoyong LuoDepartment of Oncology, The Affiliated Luoyang Central Hospital of Zhengzhou University, Luoyang, China.
Jinke YaoDepartment of General Surgery, Boji-Affiliated Hospital (Zengcheng People's Hospital), Sun Yat-Sen University, Guangzhou, China.
Peipei NieKingMed Diagnostics and KingMed School of Laboratory Medicine, Guangzhou Medical University, Guangzhou, China.
Zhiyuan YangDepartment of Medcine, The Affiliated Luoyang Central Hospital of Zhengzhou University, Luoyang, China.
Hongbo FengDepartment of Medcine, The Affiliated Luoyang Central Hospital of Zhengzhou University, Luoyang, China.
Pinjia ChenDepartment of Oncology, The Affiliated Luoyang Central Hospital of Zhengzhou University, Luoyang, China.
Xinpeng ShiDepartment of Oncology, The Affiliated Luoyang Central Hospital of Zhengzhou University, Luoyang, China.
Zhengzhi ZouMOE Key Laboratory of Laser Life Science and Institute of Laser Life Science, Joint Laboratory of Laser Oncology with Cancer Center of Sun Yat-sen University, College of Biophotonics, South China Normal University, Guangzhou, China.
Luoyang Central Hospital Affiliated to Zhengzhou University · CNGuangzhou Medical University · CNSouth China Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, to investigate whether endoplastic reticulum (ER) stress correlated with FOXM1 in colorectal cancer, we analysed the mRNA levels of FOXM1 and ER stress markers HSPA5 and spliced XBP1 by qRT-PCR. FOXM1 mRNA levels were found to positively correlate with HSPA5 in colorectal cancer. However, no significant correlation between FOXM1 and spliced XBP1 mRNA levels was found. Theses results suggested the positive correlation between FOXM1 and HSPA5 in colorectal cancer was not associated with ER stress. Next, we provided evidences that FOXM1 promoted HSPA5 transcription by directly binding to and stimulating HSPA5 promoter. Moreover, a FOXM1-binding site mapped between -1019 and -1012 bp of the proximal HSPA5 promoter was identified. In addition, we found that enhancement of cell migration and invasion by FOXM1 was significantly attenuated by depletion of HSPA5 in colorectal cancer cell. Furthermore, FOXM1 triggered colorectal cancer cell migration and invasion was involved in activities of cell-surface HSPA5. Lastly, our results suggested FOXM1 facilitated the activities and expressions of MMP2 and 9 associated with cell-surface HSPA5 in colorectal cancer cells. Moreover, statistically significant positive correlations between FOXM1 and MMP2 mRNA expression, between HSPA5 and MMP2 were found in colorectal cancer tissue specimens. Together, our results suggested that FOXM1-HSPA5 signaling might be considered as a novel molecular target for designing novel therapeutic regimen to control colorectal cancer metastasis and progression.

Indexed as

Cell Line, TumorCell MovementColorectal NeoplasmsEndoplasmic Reticulum Chaperone BiPForkhead Box Protein M1Gene Expression Regulation, NeoplasticHeat-Shock ProteinsHumansNeoplasm InvasivenessTranscriptional ActivationEndoplasmic Reticulum Chaperone BiPForkhead Box Protein M1FOXM1 protein, humanHeat-Shock ProteinsHSPA5 protein, humancolorectal cancerFOXM1HSPA5invasionmigration

Identifiers

PMID27034162
PMCPMC5041994
OpenAlexW2321000395

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.