1.A clinical study on robotic assisted laparoscopic antegrade inguinal lymphadenectomy
Hualiang YU ; Yongliang LU ; Yi XIAO ; Zhiqiang SHAO ; Jiaxiang GUO ; Yu YANG ; Hongwei WANG ; Jiangping GAO
Chinese Journal of Urology 2018;39(1):38-41
Objective To discuss the surgical strategy and clinical effects of robotic assisted laparoscopic antegrade inguinal lymphadenectomy for penile cancer.Methods We retrospectively analyzed the clinical data and surgical strategy on the 7 cases,who undergoing robotic assisted laparoscopic antegrade inguinal lymphadenectomy,from August of 2016 to August of 2017.The mean age of 7 patients was (49.7 ± 7.5) years old,ranged from 40 to 62 years old,the mean BMI was (27.97 ± 3.86) kg/m2,ranged from 21.76 to 33.21 kg/m2 . There were 4 cases of T1,2 cases of T2,1 case of T3,1 case of N1,3 cases of N2,3 cases of N3 according to TNM stages.Preoperative preparation was as follows,preoperative cardiopulmonary assessment,inguinal and pelvic CT or MRI,ultrasound of lower extremity venous,bowel preparation.The patients were placed in a supine position,with an indwelling catheter,with the head positioned lower than the hip at an angle of about 15 degrees,legs were spread apart around 45 degrees,and both knees were slightly bent and externally rotated.The da Vinci robotic patient cart was pushed forward between legs of the patient.A blunt separation was carried out between Scarpa's fascia and the surface of the aponeurosis of the obliquus externus abdominis prior,then subcutaneous space was established by a self-made balloon dilatation.Results 7 cases were completed successfully without robot reposition without any conversion.Operative time of each side ranged from 50 to 90 min (70.0 ± 12.5)min.The blood loss of each side was less than 10 ml.In the 7 cases,the number of nodes removed from left inguinal region ranged from 7 to 18 (14.0 ±3.3).The number of nodes removed from right ranged from 5 to 21 (11.0 ± 3.3).Pelvic lymphadenectomy was completed in the meantime by original trocar site on 4 cases.Till now,no perioperative complications,such as flap necrosis,delayed healing of incision,cellulitis,occurred in inguinal region,except lymphorrhagia in 3 cases.During a follow-up within 3-14 months,there was no recurrence or metastasis in 6 cases except one died from tumor progression with systemic metastasis.Conclusions Antegrade inguinal lymphadenectomy for penile cancer by using Da Vinci robotic surgical system is safe and effective.This technique also appears to diminish the wound related complications associate with the standard open approach.Compared with the similar surgery,we conducted bilateral inguinal lymphadenectomy without patient cart reposition,which simplify the procedure and reduce the using of trocar.According to individual clinical conditions,pelvic lymphadenectomy also can be completed in the meantime by original trocar.
2.Inhibition of SIRT6 in prostate cancer reduces cell viability and increases sensitivity to chemotherapeutics.
Yewei LIU ; Qian Reuben XIE ; Boshi WANG ; Jiaxiang SHAO ; Tingting ZHANG ; Tengyuan LIU ; Gang HUANG ; Weiliang XIA
Protein & Cell 2013;4(9):702-710
SIRT6 is an important histone modifying protein that regulates DNA repair, telomere maintenance, energy metabolism, and target gene expression. Recently SIRT6 has been identified as a tumor suppressor and is down-regulated in certain cancer types, but not in other cancers. From deposited gene profiling studies we found that SIRT6 was overexpressed in prostate tumors, compared with normal or paratumor prostate tissues. Tissue micro-array studies confirmed the higher levels of SIRT6 in both prostate tumor tissues and prostate cancer cells than in their normal counterparts. Knockdown of SIRT6 in human prostate cancer cells led to sub-G1 phase arrest of cell cycle, increased apoptosis, elevated DNA damage level and decrease in BCL2 gene expression. Moreover, SIRT6-deficiency reduced cell viability and enhanced chemotherapeutics sensitivity. Taken together, this study provides the first evidence of SIRT6 overexpression in human prostate cancer, and SIRT6 regulation could be exploited for prostate cancer therapy.
Apoptosis
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Cell Cycle Checkpoints
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Cell Line, Tumor
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Cell Proliferation
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Cell Survival
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DNA Damage
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Drug Resistance, Neoplasm
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Gene Knockdown Techniques
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Humans
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Male
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Prostatic Neoplasms
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genetics
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pathology
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therapy
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Proto-Oncogene Proteins c-bcl-2
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metabolism
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Sirtuins
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antagonists & inhibitors
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genetics
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metabolism
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Up-Regulation
4.Autophagy induction by SIRT6 is involved in oxidative stress-induced neuronal damage.
Jiaxiang SHAO ; Xiao YANG ; Tengyuan LIU ; Tingting ZHANG ; Qian Reuben XIE ; Weiliang XIA
Protein & Cell 2016;7(4):281-290
SIRT6 is a NAD(+)-dependent histone deacetylase and has been implicated in the regulation of genomic stability, DNA repair, metabolic homeostasis and several diseases. The effect of SIRT6 in cerebral ischemia and oxygen/glucose deprivation (OGD) has been reported, however the role of SIRT6 in oxidative stress damage remains unclear. Here we used SH-SY5Y neuronal cells and found that overexpression of SIRT6 led to decreased cell viability and increased necrotic cell death and reactive oxygen species (ROS) production under oxidative stress. Mechanistic study revealed that SIRT6 induced autophagy via attenuation of AKT signaling and treatment with autophagy inhibitor 3-MA or knockdown of autophagy-related protein Atg5 rescued H2O2-induced neuronal injury. Conversely, SIRT6 inhibition suppressed autophagy and reduced oxidative stress-induced neuronal damage. These results suggest that SIRT6 might be a potential therapeutic target for neuroprotection.
Adenine
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analogs & derivatives
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toxicity
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Autophagy
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drug effects
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Autophagy-Related Protein 5
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antagonists & inhibitors
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genetics
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metabolism
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Blotting, Western
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Cell Line, Tumor
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Humans
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Hydrogen Peroxide
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toxicity
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Microtubule-Associated Proteins
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metabolism
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Oxidative Stress
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drug effects
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Proto-Oncogene Proteins c-akt
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metabolism
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RNA Interference
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RNA, Messenger
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metabolism
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RNA, Small Interfering
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metabolism
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Reactive Oxygen Species
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metabolism
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Real-Time Polymerase Chain Reaction
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Signal Transduction
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drug effects
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Sirtuins
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antagonists & inhibitors
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genetics
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metabolism
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Transfection