Go Oshima
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View article: Cost-effectiveness analysis of pembrolizumab in patients with treatment-refractory metastatic colorectal cancer in Japan
Cost-effectiveness analysis of pembrolizumab in patients with treatment-refractory metastatic colorectal cancer in Japan Open
Objective The immune checkpoint inhibitor pembrolizumab has recently been recognized as a standard treatment regimen for patients with metastatic colorectal cancer and the microsatellite-instability-high/mismatch repair-deficient mutation.…
View article: Figure S8 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Figure S8 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Cancer cells MCF7 with strong response to 5-Aza-dC have hypermethylated MEG3-DMR promoter
View article: Figure S3 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Figure S3 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Failure of DNMT 1/3B double-knockout cells to produce liver metastases.
View article: Figure S1-S2 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Figure S1-S2 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Plasmid map of CRISPR vector and deletion schematic for CFdel cells
View article: Figure S7 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Figure S7 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Colo320 cells have limited response to 5-Aza-dC treatment and fail to produce liver metastases in vivo
View article: Figure S8 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Figure S8 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Cancer cells MCF7 with strong response to 5-Aza-dC have hypermethylated MEG3-DMR promoter
View article: Data from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Data from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Expression of 14q32-encoded miRNAs is a favorable prognostic factor in patients with metastatic cancer. In this study, we used genomic inhibition of DNA methylation through disruption of DNA methyltransferases DNMT1 and DNMT3B and pharmaco…
View article: Figure S3 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Figure S3 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Failure of DNMT 1/3B double-knockout cells to produce liver metastases.
View article: Figure S4 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Figure S4 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Viability of HCT116-L2T cells after treatment with 5-aza-dC
View article: Tables S1-S4 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Tables S1-S4 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Supplementary Tables S1-S4 show primers and gRNAs used in CRISPR/cas9 experiments and differential expression of 14q32 microRNAs in DKO mice and after treatment by 5-Aza-dC.
View article: Figure S7 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Figure S7 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Colo320 cells have limited response to 5-Aza-dC treatment and fail to produce liver metastases in vivo
View article: Supplementary Figures S5-S6 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Supplementary Figures S5-S6 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Supplemental Figures S5-S6. Distribution of CpG sites, transcription start site and methylation-dependent CTCF binding region in DLK1-MEG9 region.
View article: Figure S1-S2 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Figure S1-S2 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Plasmid map of CRISPR vector and deletion schematic for CFdel cells
View article: Tables S1-S4 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Tables S1-S4 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Supplementary Tables S1-S4 show primers and gRNAs used in CRISPR/cas9 experiments and differential expression of 14q32 microRNAs in DKO mice and after treatment by 5-Aza-dC.
View article: Data from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Data from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Expression of 14q32-encoded miRNAs is a favorable prognostic factor in patients with metastatic cancer. In this study, we used genomic inhibition of DNA methylation through disruption of DNA methyltransferases DNMT1 and DNMT3B and pharmaco…
View article: Legends to Supplementary Tables and Figures from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Legends to Supplementary Tables and Figures from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Legends to Supplementary Tables S1-S4 and Supplementary Figures S1-S8
View article: Figure S4 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Figure S4 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Viability of HCT116-L2T cells after treatment with 5-aza-dC
View article: Legends to Supplementary Tables and Figures from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Legends to Supplementary Tables and Figures from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Legends to Supplementary Tables S1-S4 and Supplementary Figures S1-S8
View article: Supplementary Figures S5-S6 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs
Supplementary Figures S5-S6 from DNA Methylation Controls Metastasis-Suppressive 14q32-Encoded miRNAs Open
Supplemental Figures S5-S6. Distribution of CpG sites, transcription start site and methylation-dependent CTCF binding region in DLK1-MEG9 region.
View article: Gamma‐synuclein is a novel prognostic marker that promotes tumor cell migration in biliary tract carcinoma
Gamma‐synuclein is a novel prognostic marker that promotes tumor cell migration in biliary tract carcinoma Open
Gamma‐synuclein (SNCG) promotes invasive behavior and is reportedly a prognostic factor in a range of cancers. However, its role in biliary tract carcinoma (BTC) remains unknown. Consequently, we investigated the clinicopathological signif…
View article: Pancreaticoduodenectomy with Non-Reconstruction of the Remnant Pancreas in Patients with Fat Replacement of the Pancreatic Tail: A Report of Two Cases
Pancreaticoduodenectomy with Non-Reconstruction of the Remnant Pancreas in Patients with Fat Replacement of the Pancreatic Tail: A Report of Two Cases Open
症例1は47歳の女性で,膵癌を疑う膵腫瘍に対し亜全胃温存膵頭十二指腸切除を施行した.膵尾部は脂肪置換され残膵断端の主膵管は同定できなかったため,膵管空腸吻合をせず膵断端を縫合し挙上空腸と膵実質を密着縫合した.術後に膵液漏は認めたが内分泌機能は良好で術後第33病日に退院した.術後2年5か月無再発で耐糖能良好である.症例2は46歳の男性で,慢性膵炎の既往がある膵神経内分泌腫瘍に対して亜全胃温存膵頭十二指腸切除を施行した.膵実質は脂肪置換され主膵管を同定できなかった.断端迅速組織…
View article: O-Glycan-Altered Extracellular Vesicles: A Specific Serum Marker Elevated in Pancreatic Cancer
O-Glycan-Altered Extracellular Vesicles: A Specific Serum Marker Elevated in Pancreatic Cancer Open
Pancreatic cancer (PC) is among the most lethal malignancies due to an often delayed and difficult initial diagnosis. Therefore, the development of a novel, early stage, diagnostic PC marker in liquid biopsies is of great significance. In …
View article: A prospective feasibility study of one-year administration of adjuvant S-1 therapy for resected biliary tract cancer in a multi-institutional trial (Tokyo Study Group for Biliary Cancer: TOSBIC01)
A prospective feasibility study of one-year administration of adjuvant S-1 therapy for resected biliary tract cancer in a multi-institutional trial (Tokyo Study Group for Biliary Cancer: TOSBIC01) Open
Background Although surgery is the definitive curative treatment for biliary tract cancer (BTC), outcomes after surgery alone have not been satisfactory. Adjuvant therapy with S-1 may improve survival in patients with BTC. This study exami…
View article: Combination of <i>KRAS</i> and <i>SMAD4</i> mutations in formalin‐fixed paraffin‐embedded tissues as a biomarker for pancreatic cancer
Combination of <i>KRAS</i> and <i>SMAD4</i> mutations in formalin‐fixed paraffin‐embedded tissues as a biomarker for pancreatic cancer Open
Formalin‐fixed paraffin‐embedded (FFPE) tissues used for routine pathological diagnosis are valuable for cancer genomic analysis; however, the association between mutation status derived from these specimens and prognosis in pancreatic duc…
View article: Usefulness of <sup>18</sup>F‐fluorodeoxyglucose positron emission tomography/computed tomography for predicting the prognosis and treatment response of neoadjuvant therapy for pancreatic ductal adenocarcinoma
Usefulness of <sup>18</sup>F‐fluorodeoxyglucose positron emission tomography/computed tomography for predicting the prognosis and treatment response of neoadjuvant therapy for pancreatic ductal adenocarcinoma Open
Background The Response Evaluation Criteria in Solid Tumors (RECIST) for computed tomography (CT) is preoperatively used to evaluate therapeutic effects. However, it does not reflect the pathological treatment response (PTR) of pancreatic …