Arunee Dechaphunkul
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Arunee Dechaphunkul has a total of 152 co-authors. Here are the top co-authors by number of shared publications:
Alexander I. Spira
23 shared publicationsAmmar Sukari
23 shared publicationsBrigette B.Y. Ma
23 shared publicationsCaroline Even
23 shared publicationsChia-Jui Yen
23 shared publicationsHongzi Liang
23 shared publications
Latest Publications
- Open Access
- 14 October 2026
- Published by MDPI AG in Current Issues in Molecular Biology
- Vol. 48 (10) , 1058
Determination of Exploratory Metastasis Biomarkers in Cancer of Unknown Primary Using Metastatic Colon Cancer as a Model: RNA Sequencing Bioinformatics Analysis
We aimed to explore the real-world practice setting and identify common genetic signaling or patterns in cancer of unknown primary (CUP) using colon cancer as a model through RNA sequencing bioinformatics analysis. Data were retrieved and analyzed using the hospital information system. We compared the number of CUP patients involved in Medical Oncology services with those who were not, and used a bioinformatics approach to analyze RNA sequencing datasets from The Cancer Genome Atlas for metastatic colon cancer as a prototype and compare information between the primary tumor and its metastatic sites. Comparisons for identifying differentially expressed genes included liver metastases versus primary tumors, lymph node metastases versus primary tumors, and all colon tumors with metastasis versus those without. Over 20 years, the hospital identified 1193 CUP patients; 154 received Medical Oncology services. We sourced 37 primary and 9 metastatic (5 liver, 4 lymph node) colon cancer RNA sequencing datasets for bioinformatics analysis. Multigroup analysis identified ROPN1, Y_RNA, and OR4F4 as highly expressed in both metastatic types. High ROPN1 expression was associated with poor overall and disease-free survival rates. RNA sequencing bioinformatics is potentially useful for identifying exploratory metastasis biomarkers in CUP. ROPN1 may be linked to metastasis and unfavorable prognosis in colon cancer. Further analysis across paired primary/metastatic panels from multiple cancer types is warranted to determine the lineage-tracing utility in CUP.
- 14 October 2026
- Published by MDPI AG in Current Issues in Molecular Biology
- Vol. 48 (10) , 1058
Open AccessDetermination of Exploratory Metastasis Biomarkers in Cancer of Unknown Primary Using Metastatic Colon Cancer as a Model: RNA Sequencing Bioinformatics Analysis
We aimed to explore the real-world practice setting and identify common genetic signaling or patterns in cancer of unknown primary (CUP) using colon cancer as a model through RNA sequencing bioinformatics analysis. Data were retrieved and analyzed using the hospital information system. We compared the number of CUP patients involved in Medical Oncology services with those who were not, and used a bioinformatics approach to analyze RNA sequencing datasets from The Cancer Genome Atlas for metastatic colon cancer as a prototype and compare information between the primary tumor and its metastatic sites. Comparisons for identifying differentially expressed genes included liver metastases versus primary tumors, lymph node metastases versus primary tumors, and all colon tumors with metastasis versus those without. Over 20 years, the hospital identified 1193 CUP patients; 154 received Medical Oncology services. We sourced 37 primary and 9 metastatic (5 liver, 4 lymph node) colon cancer RNA sequencing datasets for bioinformatics analysis. Multigroup analysis identified ROPN1, Y_RNA, and OR4F4 as highly expressed in both metastatic types. High ROPN1 expression was associated with poor overall and disease-free survival rates. RNA sequencing bioinformatics is potentially useful for identifying exploratory metastasis biomarkers in CUP. ROPN1 may be linked to metastasis and unfavorable prognosis in colon cancer. Further analysis across paired primary/metastatic panels from multiple cancer types is warranted to determine the lineage-tracing utility in CUP.
- Open Access
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S2 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Baseline immune cell subset associations with objective response rate
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S2 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Baseline immune cell subset associations with objective response rate
- Open Access
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S4 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Kaplan-Meier plots for baseline immunohistochemistry biomarker associations
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S4 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Kaplan-Meier plots for baseline immunohistochemistry biomarker associations
- Open Access
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S3 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Baseline prevalence and clinical response associations in immune cell subsets
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S3 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Baseline prevalence and clinical response associations in immune cell subsets
- Open Access
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S6 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Association between ctDNA and clinical response
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S6 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Association between ctDNA and clinical response
- Open Access
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S7 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Longitudinal analysis of regulatory T-cell dynamics following tobemstomig or nivolumab treatment
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S7 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Longitudinal analysis of regulatory T-cell dynamics following tobemstomig or nivolumab treatment
- Open Access
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S5 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Baseline tissue gene expression and gene signature associations with clinical outcomes
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S5 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Baseline tissue gene expression and gene signature associations with clinical outcomes
- Open Access
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Table S2 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Immunohistochemistry and immunofluorescent assay details
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Table S2 from A Randomized, Nivolumab-Controlled, Phase II Biomarker Study of Lomvastomig and Tobemstomig in Advanced or Metastatic Squamous Cell Carcinoma of the Esophagus
Immunohistochemistry and immunofluorescent assay details