Evidence map›Paper›PMID 26104296›Full record

ArticleJournal of translational medicine2015

The prognostic significance of CXCL1 hypersecretion by human colorectal cancer epithelia and myofibroblasts.

Anne-France le Rolle, Thang K Chiu, Michael Fara, Jinru Shia, Zhaoshi Zeng, Martin R Weiser, Philip B Paty, Vi K Chiu

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

36 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. The Significance of CXCL1 in Cancer: An Overview of Molecular Mechanisms.International journal of molecular sciences · 2026
    Review
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  14. Expression and Prognostic Role of CXCL1 Gene in Colorectal Adenocarcinoma.Computational intelligence and neuroscience · 2022
    Article
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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 4 institutions in 1 country.

Anne-France le RolleDivision of Hematology/Oncology and Chao Family Comprehensive Cancer Center, Department of Medicine, University of California, 839 Health Sciences Road, Sprague Hall Office 116, Irvine, CA, 92697, USA. alerolle@uci.edu.
Thang K ChiuDepartment of Biochemistry and Molecular Biology, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA. thangchiu@yahoo.com.
Michael FaraDepartment of Medicine, Weill Cornell Medical College, New York, NY, 10065, USA. michael.fara@gmail.com.
Jinru ShiaDepartment of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY, 10065, USA. shiaj@mskcc.org.
Zhaoshi ZengDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY, 10065, USA. zengz@mskcc.org.
Martin R WeiserDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY, 10065, USA. weiser1@mskcc.org.
Philip B PatyDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY, 10065, USA. patyp@mskcc.org.
Vi K ChiuDivision of Hematology/Oncology and Chao Family Comprehensive Cancer Center, Department of Medicine, University of California, 839 Health Sciences Road, Sprague Hall Office 116, Irvine, CA, 92697, USA. vkchiu@uci.edu.
Memorial Sloan Kettering Cancer Center · USUniversity of California, Irvine · USCornell University · USLouisiana State University Health Sciences Center New Orleans · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Christine Hui · 1994 to 2026
$57.9M
NCI NIH HHS P01CA655930-05A2NCI NIH HHS P30 CA062203NCI NIH HHS P30CA062203
6 · The paper itself

Abstract

backgroundClinical therapy for metastatic colorectal cancer (CRC) remains limited, especially when the tumor harbors a KRAS mutation. This study aimed to identify prognostic biomarkers in CRC that are accessible for therapeutic inhibition.

methodsConditioned media from human CRC epithelial cells and myofibroblasts were screened by cytokine arrays for tumorigenic factors. The protein and mRNA expressions of these factors were determined by immunohistochemistry and gene microarrays in human CRC tissues. Prognostic biomarkers were determined by correlation of mRNA expression to overall survival in stage IV CRC patients. Inhibition of CXCL1 was performed with specific neutralizing antibody and lentiviral shRNAs. Malignant growth was assessed by soft agar growth assays and xenograft tumor growth in immunocompromised mice.

resultsCXCL1 was highly secreted by KRAS mutant human CRC cells and myofibroblasts in a complementary adaptive response to serum deprivation. Elevated CXCL1 level promoted anchorage-independent growth of murine fibroblasts and human CRC cells. Inhibition of CXCL1 by neutralizing antibody and specific shRNAs decreased CRC tumor growth. Highly elevated CXCL1 expression significantly correlated with decreased overall survival in stage IV CRC patients (hazard ratio 0.28; 95% CI 0.11-0.72).

conclusionsHigh CXCL1 expression is a poor prognostic biomarker in metastatic CRC. CXCL1 inhibition suppressed tumorigenic growth of KRAS mutant CRC cells.

Indexed as

AdultAgedAged, 80 and overAnimalsCarcinogenesisCell Line, TumorCell ProliferationChemokine CXCL1Colorectal NeoplasmsCulture Media, ConditionedEpithelial CellsEpitheliumFemaleGene Expression Regulation, NeoplasticHumansInterleukin-8Chemokine CXCL1Culture Media, ConditionedCXCL1 protein, humanInterleukin-8RNA, Messenger

Identifiers

PMID26104296
PMCPMC4477596
OpenAlexW2165354808

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.