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1.
Sci Rep ; 14(1): 22458, 2024 09 28.
Article in English | MEDLINE | ID: mdl-39342001

ABSTRACT

With the continuous development of robot-assisted technology, Robot-assisted Laparoscopic Partial Nephrectomy (RALPN) has gradually become an optional method for the treatment of Hemorrhage secondary to angiomyolipoma (HSA). However, there are rare clinical reports of the primary RALPN for HSA. Therefore, this research aims to evaluate the efficacy and safety of primary RALPN for HSA. Fourteen patients(six males and eight females), aged 14-56 years, underwent primary RALPN for HSA and were retrospectively analyzed from 2015 to 2023. The initial blood routine examination revealed decreased hemoglobin in all patients, and Contrast-enhanced computed tomography (CT) indicated retroperitoneal hematoma. After correcting shock and electrolyte imbalance through fluid therapy and medical treatment, all primary RALPN procedures were performed with transabdominal access on the side of the Hemorrhage. After tumor resection and hematoma removal with a monopolar Curved Scissor, the absorbable barbed suture was performed for inner and outer running stitches, respectively. Patient demographic information, perioperative characteristics, and functional outcomes were collected and analyzed. The initial tumor size of fourteen patients ranged from 57 to 145 mm, and the RENAL ranged from 7 to 11. All of the HSA was controlled, and primary RALPN was successful. The operating time it was ranged from 105 to 265 min. Postoperatively, one patient exhibited chylous drainage (Clavien-Dindo II), and another patient developed pleural effusion (Clavien-Dindo III). No postoperative transfusion and Digital Subtraction Angiography (DSA) highly selective embolization of the bleeding vessel was needed. No patients developed urinoma or urinary fistula. Within the follow-up period, the overall complications were manageable. Primary RALPN is a safe and effective procedure for HSA, which may be considered an alternative to selective renal artery embolization.


Subject(s)
Angiomyolipoma , Kidney Neoplasms , Laparoscopy , Nephrectomy , Robotic Surgical Procedures , Tertiary Care Centers , Humans , Female , Angiomyolipoma/surgery , Angiomyolipoma/complications , Male , Nephrectomy/methods , Nephrectomy/adverse effects , Adult , Middle Aged , Retrospective Studies , Laparoscopy/methods , Laparoscopy/adverse effects , Robotic Surgical Procedures/methods , Robotic Surgical Procedures/adverse effects , China , Adolescent , Kidney Neoplasms/surgery , Kidney Neoplasms/complications , Young Adult , Hemorrhage/etiology , Hemorrhage/surgery , Treatment Outcome
2.
Cell Cycle ; 21(9): 984-1002, 2022 05.
Article in English | MEDLINE | ID: mdl-35167417

ABSTRACT

Cervical carcinoma is a leading malignant tumor among women worldwide, characterized by the dysregulation of cell cycle. Cyclin-dependent kinase 6 (CDK6) plays important roles in the cell cycle progression, cell differentiation, and tumorigenesis. However, the role of CDK6 in cervical cancer remains controversial. Here, we found that loss of CDK6 in cervical adenocarcinoma HeLa cell line inhibited cell proliferation but induced apoptosis as well as autophagy, accompanied by attenuated expression of mammalian target of rapamycin complex 1 (mTORC1) and hexokinase 2 (HK2), reduced glycolysis, and production of protein, nucleotide, and lipid. Similarly, we showed that CDK6 knockout inhibited the survival of CDK6-high CaSki but not CDK6-low SiHa cervical cancer cells by regulation of glycolysis and autophagy process. Collectively, our studies indicate that CDK6 is a critical regulator of human cervical cancer cells, especially with high CDK6 level, through its ability to regulate cellular apoptosis and metabolism. Thus, inhibition of CDK6 kinase activity could be a powerful therapeutic avenue used to treat cervical cancers.


Subject(s)
Cyclin-Dependent Kinase 6 , Uterine Cervical Neoplasms , Apoptosis , Autophagy , Cell Line, Tumor , Cell Proliferation , Female , Glycolysis , HeLa Cells , Hexokinase/genetics , Hexokinase/metabolism , Humans , Male , Mechanistic Target of Rapamycin Complex 1/metabolism , Uterine Cervical Neoplasms/pathology
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