Evidence map›Paper›PMID 26767044›Full record

ArticleThoracic cancer2014

Apolipoprotein C1 (APOC1) as a novel diagnostic and prognostic biomarker for lung cancer: A marker phase I trial.

Hui-Ling Ko, Yu-Shan Wang, Weng-Lam Fong, Mau-Shin Chi, Kwan-Hwa Chi, Shang-Jyh Kao

Open access · bronzeAbstract read
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Article in Thoracic cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

47 citing papers in PubMed, 73 citations in OpenAlex.

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  20. Apolipoproteins: New players in cancers.Frontiers in pharmacology · 2022
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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

6 authors at 2 institutions in 1 country.

Hui-Ling KoDepartment of Radiation Therapy and Oncology, Shin Kong Wu Ho-Su Memorial Hospital Taipei, Taiwan.
Yu-Shan WangDepartment of Radiation Therapy and Oncology, Shin Kong Wu Ho-Su Memorial Hospital Taipei, Taiwan.
Weng-Lam FongDepartment of Radiation Therapy and Oncology, Shin Kong Wu Ho-Su Memorial Hospital Taipei, Taiwan.
Mau-Shin ChiDepartment of Radiation Therapy and Oncology, Shin Kong Wu Ho-Su Memorial Hospital Taipei, Taiwan.
Kwan-Hwa ChiDepartment of Radiation Therapy and Oncology, Shin Kong Wu Ho-Su Memorial Hospital Taipei, Taiwan.
Shang-Jyh KaoDivision of Chest Medicine, Shin Kong Wu Ho-Su Memorial Hospital Taipei, Taiwan.
Memorial Hospital of South Bend · USMemorial Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumor cells continuously evolve over time in response to host pressures. However, explanations as to how tumor cells are influenced by the inflammatory tumor microenvironment over time are, to date, poorly defined. We hypothesized that prognostic biomarkers could be obtained by exploring the expression of inflammation-associated genes between early and late stage lung cancer tumor samples.

methodsCandidate inflammation-associated genes, apolipoprotein C-1 (APOC1), MMP1, KMO)1, CXCL5, CXCL)7, IL-1α, IL-1β, TNF-α and IL-6 were verified by real-time quantitative polymerase chain reaction. Gene expression profiles and immunofluorescence staining of 30 lung cancer tissues were compared.

resultsExpressions of APOC1 and IL-6 mRNA on tumor tissues in late stage disease were significantly higher than in early stage lung cancer samples. Immunofluorescence staining of tumor samples showed that the expression of APOC1 gradually increased from early to late stage in lung cancer patients. The expression levels of IL-6 and APOC1 in tumor samples were positively correlated; however, no prognostic value of APOC1 can be identified in serum samples.

conclusionsWe found that the level of tumor APOC1 was highly expressed in late stage lung cancer. Further research is warranted to determine the molecular mechanisms underlying the cross talk of APOC1 and IL-6 in tumor progression. An expanded sample size marker phase II study may lead to the discovery of new lung cancer therapeutics targeting APOC1.

Indexed as

APOC1gene-expression profilinginflammation-associated geneslung cancerRT-PCR

Identifiers

PMID26767044
PMCPMC4704334
OpenAlexW1501950022

What OpenQuestion holds

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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.