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1.
Int J Gynecol Cancer ; 27(9): 1990-1999, 2017 11.
Article in English | MEDLINE | ID: mdl-28858908

ABSTRACT

OBJECTIVE: The aim of this study was to compare the surgical outcomes of robotic-assisted radical hysterectomy (RRH) with traditional laparoscopic radical hysterectomy (TLRH) for the treatment of early-stage cervical cancer in a large retrospective cohort of a total of 933 patients. METHODS: We have enrolled 100 patients into the RRH and 833 patients into the TLRH group. The surgical outcomes include operating time, blood loss, transfusion rate, pelvic lymph node yield, hospitalization days, duration of bowel function recovery, catheter removal before and after 3 weeks, conversion to laparotomy, and intraoperative and postoperative complications. Follow-up results were also analyzed for all patients. RESULTS: Both groups have similar patient and tumor characteristics but patients with a larger lesion size were preferably enrolled in the TLRH treatment group. The treatment with RRH was generally superior to TLRH with respect to operating time, blood loss, length of hospitalization, duration of bowel function recovery, and postoperative complications. On follow-up of patients, there were no relapses reported in the RRH group compared with 4% of relapse cases and 2.9% of deaths because of metastasis in the TLRH group. No conversion of laparotomy occurred in the RRH group. No significant difference was found with respect to intraoperative complications and blood transfusion between both groups. CONCLUSIONS: The results from this study suggest that RRH is superior to TLRH with regard to surgical outcome and may pose a safe and feasible alternative to TLRH. The operating time and lymph node yield is acceptable. Our study is one of the largest single-center studies of surgical outcomes comparing RRH with TLRH during cervical cancer treatment and will significantly contribute to the safety of alternative treatment options for patients. Furthermore, the difference detected between TLRH and RRH group is further strengthened by the great expertise of the surgeon performing laparoscopic surgeries.


Subject(s)
Hysterectomy/methods , Uterine Cervical Neoplasms/surgery , Female , Humans , Hysterectomy/adverse effects , Laparoscopy/adverse effects , Laparoscopy/methods , Middle Aged , Postoperative Complications/etiology , Retrospective Studies , Robotic Surgical Procedures/adverse effects , Robotic Surgical Procedures/methods , Treatment Outcome
2.
EBioMedicine ; 11: 91-100, 2016 Sep.
Article in English | MEDLINE | ID: mdl-27522322

ABSTRACT

Similar to estrogens, bone morphogenetic protein 4 (BMP4) promotes the accumulation of more metabolically active subcutaneous fat and reduction of visceral fat. However, whether there is a cross-talk between BMP4 and estrogen signaling remained unknown. Herein, we found that BMP4 deficiency in white adipose tissue (WAT) increased the estrogen receptor α (ERα) level and its signaling, which prevented adult female mice from developing high fat diet (HFD)-induced obesity and insulin resistance; estrogens depletion up regulated BMP4 expression to overcome overt adiposity and impaired insulin sensitivity with aging, and failure of BMP4 regulation due to genetic knockout led to more fat gain in aged female mice. This mutual regulation between BMP4 and estrogen/ERα signaling may also happen in adipose tissue of women, since the BMP4 level significantly increased after menopause, and was inversely correlated with body mass index (BMI). These findings suggest a counterbalance between BMP4 and estrogen/ERα signaling in the regulation of adiposity and relative metabolism in females.


Subject(s)
Adiposity , Bone Morphogenetic Protein 4/metabolism , Estrogen Receptor alpha/metabolism , Estrogens/metabolism , Glucose/metabolism , Signal Transduction , Adipocytes/metabolism , Adipose Tissue/metabolism , Adiposity/genetics , Age Factors , Animals , Body Mass Index , Bone Morphogenetic Protein 4/genetics , Cell Line , Diet, High-Fat , Estrogens/pharmacology , Female , Gene Expression Regulation , Humans , Insulin Resistance , Metabolic Diseases/metabolism , Mice , Mice, Knockout , Models, Animal , Obesity/metabolism , Protein Binding , Protein Stability
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