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Asian J Endosc Surg ; 16(2): 163-172, 2023 Apr.
Article in English | MEDLINE | ID: mdl-36127882

ABSTRACT

INTRODUCTION: Compared with laparoscopic surgery (LS), robotic surgery (RS) is considered to have acceptable outcomes in rectal cancer, but few reports have focused on chylous ascites in RS. The aim of this study was to investigate the incidence and etiology of chylous ascites after RS. METHODS: This retrospective study included 291 patients with rectal cancer who underwent RS (n = 165) or LS (n = 126) with high ligation of the inferior mesenteric artery (IMA). Propensity score matching (PSM) was performed to compare the two groups. RESULTS: \Dissection around the IMA was achieved using ultrasonic coagulating shears in most LS cases, and monopolar scissors in most RS cases, sometimes using bipolar vessel sealing device or bipolar forceps. The incidence of chylous ascites was 12.2% in RS and 4.1% in LS after PSM (P = .037). When limited to the RS group, multivariate analysis identified absence of lymphatic sealing at the left side of the IMA and shorter operative time as independent risk factors for chylous ascites. Except for duration of drain placement, no outcomes differed significantly with or without chylous ascites. One patient with chylous ascites developed later infection and required antibiotic treatment. CONCLUSION: The incidence of chylous ascites is significantly higher in RS than in LS, and RS with incomplete lymphatic sealing around the IMA is a risk factor for chylous ascites in rectal cancer. Although outcomes for patients with chylous ascites were acceptable, adequate lymphatic sealing during dissection around the IMA is crucial to prevent chylous ascites in RS.


Subject(s)
Chylous Ascites , Laparoscopy , Rectal Neoplasms , Robotic Surgical Procedures , Humans , Robotic Surgical Procedures/adverse effects , Mesenteric Artery, Inferior/surgery , Chylous Ascites/epidemiology , Chylous Ascites/etiology , Chylous Ascites/surgery , Retrospective Studies , Rectal Neoplasms/surgery , Rectal Neoplasms/complications , Risk Factors , Laparoscopy/adverse effects
2.
Virchows Arch ; 479(2): 277-284, 2021 Aug.
Article in English | MEDLINE | ID: mdl-33638656

ABSTRACT

Colorectal cancer (CRC) is one of the most common gastrointestinal cancers worldwide with high morbidity and mortality rates. The discovery of small molecule anticancer reagents has significantly affected cancer therapy. However, the anticancer effects of these therapies are not sufficient to completely cure CRC. PDZ-binding kinase (PBK) was initially identified as a mitotic kinase for mitogen-activated protein kinase and is involved in cytokinesis and spermatogenesis. Aberrant expression of PBK has been reported to be closely associated with malignant phenotypes of many cancers and/or patient survival. However, the expression of PBK and its association to patient survival in CRC have not been fully elucidated. In the present study, 269 primary CRCs were evaluated immunohistochemically for PBK expression to assess its ability as a prognostic factor. CRC tumor cells variably expressed PBK (range, 0-100%; median, 32%) in the nucleus and cytoplasm. Univariate analyses identified a significant inverse correlation between PBK expression and pT stage (P<0.0001). Furthermore, patients carrying CRC with higher PBK expression showed significantly favorable survival (P=0.0094). Multivariate Cox proportional hazards regression analysis revealed high PBK expression (HR, 0.52; P=0.015) as one of the potential favorable factors for CRC patients. PBK expression showed significant correlation to Ki-67 labeling indices (ρ=0.488, P<0.0001). In vitro, the PBK inhibitor OTS514 suppressed cellular proliferation of CRC cells with PBK expression through downregulation of P-ERK and induction of apoptosis. These results suggest that PBK-targeting therapeutics may be useful for the treatment of PBK-expressing CRC patients.


Subject(s)
Biomarkers, Tumor/metabolism , Colorectal Neoplasms/enzymology , Mitogen-Activated Protein Kinase Kinases/metabolism , Aged , Aged, 80 and over , Antineoplastic Agents/pharmacology , Apoptosis/drug effects , Biomarkers, Tumor/antagonists & inhibitors , Caco-2 Cells , Cell Proliferation/drug effects , Colorectal Neoplasms/mortality , Colorectal Neoplasms/pathology , Colorectal Neoplasms/therapy , Extracellular Signal-Regulated MAP Kinases/metabolism , Female , HCT116 Cells , Humans , Immunohistochemistry , Male , Middle Aged , Mitogen-Activated Protein Kinase Kinases/antagonists & inhibitors , Neoplasm Staging , Phosphorylation , Protein Kinase Inhibitors/pharmacology , Quinolones/pharmacology , Risk Assessment , Risk Factors , Thiophenes/pharmacology , Time Factors , Treatment Outcome
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