Naoko Goto-Inoue

Dr. Naoko Goto-Inoue

Department of Marine Science and Resources, College of Bioresource Sciences, Nihon University, 1866 Kameino, Fujisawa, Kanagawa 252-0880, Japan

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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Journal Article
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NZNOBUHIRO ZAIMA
NOBUHIRO ZAIMA
THTakahiro Hayasaka
Takahiro Hayasaka
NGNaoko Goto-Inoue
Naoko Goto-Inoue
MSMitsutoshi Setou
Mitsutoshi Setou
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) is a powerful tool that enables the simultaneous detection and identification of biomolecules in analytes. MALDI-imaging mass spectrometry (MALDI-IMS) is a two-dimensional MALDI-mass spectrometric technique used to visualize the spatial distribution of biomolecules without extraction, purification, separation, or labeling of biological samples. MALDI-IMS has revealed the characteristic distribution of several biomolecules, including proteins, peptides, amino acids, lipids, carbohydrates, and nucleotides, in various tissues. The versatility of MALDI-IMS has opened a new frontier in several fields such as medicine, agriculture, biology, pharmacology, and pathology. MALDI-IMS has a great potential for discovery of unknown biomarkers. In this review, we describe the methodology and applications of MALDI-IMS for biological samples.

19 June 2009 in Glycobiology
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NGNaoko Goto-Inoue
Naoko Goto-Inoue
THTakahiro Hayasaka
Takahiro Hayasaka
NZNobuhiro Zaima
Nobuhiro Zaima
MSMitsutoshi Setou
Mitsutoshi Setou
More than 90% of the glycolipid in mammalian testis consists of a unique sulfated glyceroglycolipid called seminolipid. The galactosylation of the molecule is catalyzed by UDP-galactose:ceramide galactosyltransferase (CGT). Disruption of the CGT gene in mice results in male infertility due to the arrest of spermatogenesis, indicating that seminolipid plays an important role in reproductive function. Seminolipid molecules can be assigned to different molecular species based on the fatty acid composition. In this report, we investigated the localizations of the molecular species of seminolipid by imaging mass spectrometry and demonstrated that major molecule (C16:0-alkyl-C16:0-acyl) was expressed throughout the tubules: some (C16:0-alkyl-C14:0-acyl and C14:0-alkyl-C16:0-acyl) were predominantly expressed in spermatocytes and the other (C17:0-alkyl-C16:0-acyl) was specifically expressed in spermatids and spermatozoa. This is the first report to show the cell-specific localization of each molecular species of seminolipid during testicular maturation.

10 August 2010 in Journal of the American Society for Mass Spectrometry
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Journal Article
Closed access
NGNaoko Goto-Inoue
Naoko Goto-Inoue
THTakahiro Hayasaka
Takahiro Hayasaka
NZNobuhiro Zaima
Nobuhiro Zaima
YKYukiyasu Kashiwagi
Yukiyasu Kashiwagi
MYMari Yamamoto
Mari Yamamoto
MSMitsutoshi Setou
Mitsutoshi Setou

1 October 2009 in Journal of Chromatography A
Verified
Journal Article
Closed access
NGNaoko Goto-Inoue
Naoko Goto-Inoue
THTakahiro Hayasaka
Takahiro Hayasaka
TTTakao Taki
Takao Taki
TGTania Valdes Gonzalez
Tania Valdes Gonzalez
MSMitsutoshi Setou
Mitsutoshi Setou

2 December 2019 in Foods
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MMMizuki Morisasa
Mizuki Morisasa
TSTomohiko Sato
Tomohiko Sato
KKKeisuke Kimura
Keisuke Kimura
TMTsukasa Mori
Tsukasa Mori
NGNaoko Goto-Inoue
Naoko Goto-Inoue
Food contains various compounds, and there are many methods available to analyze each of these components. However, the large amounts of low-molecular-weight metabolites in food, such as amino acids, organic acids, vitamins, lipids, and toxins, make it difficult to analyze the spatial distribution of these molecules. Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) imaging is a two-dimensional ionization technology that allows the detection of small metabolites in tissue sections without requiring purification, extraction, separation, or labeling. The application of MALDI-MS imaging in food analysis improves the visualization of these compounds to identify not only the nutritional content but also the geographical origin of the food. In this review, we provide an overview of some recent applications of MALDI-MS imaging, demonstrating the advantages and prospects of this technology compared to conventional approaches. Further development and enhancement of MALDI-MS imaging is expected to offer great benefits to consumers, researchers, and food producers with respect to breeding improvement, traceability, the development of value-added foods, and improved safety assessments.

24 February 2011 in Cancer Science
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TSTomohiko Setoguchi
Tomohiko Setoguchi
HKHirotoshi Kikuchi
Hirotoshi Kikuchi
MYMasayoshi Yamamoto
Masayoshi Yamamoto
MBMegumi Baba
Megumi Baba
MOManabu Ohta
Manabu Ohta
HKHiroyuki Konno
Hiroyuki Konno
Although the main cause of gastrointestinal stromal tumor (GIST) is gain‐of‐function mutations in thec‐kitgene in the interstitial cells of Cajal, concomitant genetic or epigenetic changes other thanc‐kitappear to occur in the development of metastasis. We sought to identify the genes involved in the metastatic process of gastric GIST. Microarray analysis was performed to compare gene expressions between three gastric GIST and four metastatic liver GIST. Expression levels were higher for 165 genes and lower for 146 genes in metastatic liver GIST. The upregulation of five oncogenes and downregulation of four tumor suppressor genes including versican and CD9 were confirmed by quantitative reverse transcriptional PCR. Immunohistochemistry in 117 GIST revealed that protein levels of versican and CD9 were higher and lower, respectively, in metastatic GIST. High expression of versican and low expression of CD9 in 104 primary gastric GIST correlated with poor disease‐free survival (P = 0.0078 andP = 0.0018). In addition to thec‐kitgene mutation, genetic or epigenetic changes other thanc‐kitplay important roles in the metastatic process. In particular, versican and CD9 are potential prognostic markers in gastric GIST. (Cancer Sci2011; 102: 883–889)