Evidence map›Paper›PMID 31035594›Full record

ArticleCancers2019

Comprehensive Serum Glycopeptide Spectra Analysis (CSGSA): A Potential New Tool for Early Detection of Ovarian Cancer.

Masaru Hayashi, Koji Matsuo, Kazuhiro Tanabe, Masae Ikeda, Mariko Miyazawa, Miwa Yasaka, Hiroko Machida, Masako Shida, Tadashi Imanishi, Brendan H Grubbs and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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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 2 institutions in 2 countries.

Masaru HayashiDepartment of Obstetrics and Gynecology, Tokai University School of Medicine, Kanagawa 2591193, Japan. hayashimasaru0620@hotmail.com.
Koji MatsuoDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Southern California, Los Angeles, CA 90033, USA. koji.matsuo@med.usc.edu.
Kazuhiro TanabeMedical Solution Promotion Department, LSI Medience Corporation, Tokyo 1748555, Japan. tanabe.kazuhiro@mp.medience.co.jp.
Masae IkedaDepartment of Obstetrics and Gynecology, Tokai University School of Medicine, Kanagawa 2591193, Japan. ikedam@tokai-u.jp.
Mariko MiyazawaDepartment of Obstetrics and Gynecology, Tokai University School of Medicine, Kanagawa 2591193, Japan. marikom@tokai-u.jp.
Miwa YasakaDepartment of Obstetrics and Gynecology, Tokai University School of Medicine, Kanagawa 2591193, Japan. mm_4amm1302@yahoo.co.jp.
Hiroko MachidaDepartment of Obstetrics and Gynecology, Tokai University School of Medicine, Kanagawa 2591193, Japan. hiroko.machida@tokai.ac.jp.
Masako ShidaDepartment of Obstetrics and Gynecology, Tokai University School of Medicine, Kanagawa 2591193, Japan. shida@is.icc.u-tokai.ac.jp.
Tadashi ImanishiDepartment of Molecular Life Science, Division of Basic Medical Science and Molecular Medicine, Tokai University School of Medicine, Kanagawa 2591193, Japan. imanishi@tokai-u.jp.ORCID 0000-0002-1182-9127
Brendan H GrubbsDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Southern California, Los Angeles, CA 90027, USA. brendan.grubbs@med.usc.edu.
Takeshi HirasawaDepartment of Obstetrics and Gynecology, Tokai University School of Medicine, Kanagawa 2591193, Japan. hira@is.icc.u-tokai.ac.jp.ORCID 0000-0002-4009-1758
Mikio MikamiDepartment of Obstetrics and Gynecology, Tokai University School of Medicine, Kanagawa 2591193, Japan. mmikami@is.icc.u-tokai.ac.jp.ORCID 0000-0002-7496-3518
Tokai University · JPUniversity of Southern California · US

Funding

Grant-in-aid for scientific research from Ministry of Education, Culture, Sports, Science and Technology 17H04340, 18K09274, 18K09300Mr. Minoru Sano Memorial Fund and Tokai University Research Aid n/a
6 · The paper itself

Abstract

objectivesTo conduct a comprehensive glycopeptide spectra analysis of serum between cancer and non-cancer patients to identify early biomarkers of epithelial ovarian cancer (EOC).

methodsApproximately 30,000 glycopeptide peaks were detected from the digested serum glycoproteins of 39 EOC patients (23 early-stage, 16 advanced-stage) and 45 non-cancer patients (27 leiomyoma and ovarian cyst cases, 18 endometrioma cases) by liquid chromatography mass spectrometry (LC-MS). The differential glycopeptide peak spectra were analyzed to distinguish between cancer and non-cancer groups by employing multivariate analysis including principal component analysis (PCA), orthogonal partial least squares discriminant analysis (OPLS-DA) and heat maps.

resultsExamined spectral peaks were filtered down to 2281 serum quantitative glycopeptide signatures for differentiation between ovarian cancer and controls using multivariate analysis. The OPLS-DA model using cross-validation parameters R2 and Q2 and score plots of the serum samples significantly differentiated the EOC group from the non-cancer control group. In addition, women with early-stage clear cell carcinoma and endometriomas were clearly distinguished from each other by OPLS-DA as well as by PCA and heat maps.

conclusionsOur study demonstrates the potential of comprehensive serum glycoprotein analysis as a useful tool for ovarian cancer detection.

Indexed as

comprehensive serum glycopeptide spectra analysisendometriomaepithelial ovarian cancerorthogonal partial square discrimination analysisovarian clear cell carcinoma

Identifiers

PMID31035594
PMCPMC6563019
OpenAlexW2940764668

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.