1.Retrospective analysis of treatment for severe ovary hyperstimulation syndrome complicated by pleural effusion and ascites.
Fei GONG ; Hui GUO ; Yan SHEN ; Juan LI ; Guangxiu LU ; Ge LIN
Journal of Central South University(Medical Sciences) 2012;37(7):720-724
OBJECTIVE:
To investigate the effectiveness of treatment for severe ovary hyperstimulation syndrome (OHSS) complicated by pleural effusion and ascites after in vitro fertilization preembryo transfer (IVF-ET).
METHODS:
One hundred and thirty-two patients with severe OHSS in our hospital (from January 2007 to December 2010) were retrospectively analyzed and the efficacy of three therapeutic methods was compared. Twenty-five patients in group I were treated with low-molecular dextran and albumin, 67 patients in group II were treated with 6% medium molecular-weight hydroxyethyl starch, and 40 patients in group III were treated with active aspiration of pleural effusion and ascites.
RESULTS:
All three therapies improved the symptoms of OHSS and various blood biochemical parameters. The duration of hospitalization of group III [(7.4±4.5) d] was significantly less than those of group I [(21.4±9.2) d] or II [(15.6±6.7) d], and the cost of group III [(2656.2±1882.8) Yuan] was also significantly lower than that of group I or II [(11937.6±7989.8) and (5182.7±2991.7) Yuan, respectively].
CONCLUSION
Abdominal B ultrasonography-guided trans-abdominal wall aspiration of pleural effusion and ascites combined with blood volume maintenance is an effective and economical way to treat OHSS.
Adult
;
Ascites
;
etiology
;
therapy
;
Dextrans
;
administration & dosage
;
Drainage
;
Female
;
Fertilization in Vitro
;
Humans
;
Hydroxyethyl Starch Derivatives
;
administration & dosage
;
Infusions, Intravenous
;
Ovarian Hyperstimulation Syndrome
;
complications
;
therapy
;
Ovulation Induction
;
adverse effects
;
Pleural Effusion
;
etiology
;
therapy
;
Retrospective Studies
;
Serum Albumin
;
administration & dosage
2.Effects of long non-coding RNA TUG1 on the proliferation and apoptosis of gastric cancerAGS cells
LIU Shiping ; XIE Junfeng ; WU Xiaojuan ; XIE Ningsheng ; TANG Jianhua ; GUO Guangxiu
Chinese Journal of Cancer Biotherapy 2019;26(11):1256-1261
Objective: To investigate the expression of lncRNA TUG1 (long non-coding RNA taurine up-regulated gene 1) in gastric cancer and its effect on the proliferation and apoptosis of gastric cancer cells. Methods: Surgically resected gastric cancer tissues and corresponding distal normal tissues (>5 cm away from the margin of tumor) of 40 gastric cancer patients from March 2016 to December 2017 at Ganzhou People's Hospital of Jiangxi Province were collected, and qPCR was used to examine the expression of lncRNA TUG1.AGS gastric cancer cells were transfected with lncRNATUG1 over-expression plasmids and siRNAs, and the effects of lncRNA TUG1 on cell proliferation and apoptosis were assessed by CCK-8, qPCR and Flow cytometry. Results: lncRNATUG1 expression was significantly increased in gastric cancer tissues as compared to normal tissues; and it was not correlated with gender, age, tumor size, infiltration depth of tumor, lymph node-metastasis, tumor differentiation and TNM staging. TUG1 over-expression significantly suppressed the expressions of CDKN1A, BAX and Caspase-3 in AGS gastric cancer cells, and decreased G1 phase proportion and apoptosis rate, but increased S phase proportion and cell viability; in contrast, TUG1 siRNA transfection significantly promoted the expressions of CDKN1A, BAX and Caspase-3, and increased G1 phase proportion and apoptosis rate, but decreased S phase proportion and cell viability. Conclusion: Up-regulated lncRNATUG1 promotes proliferation and inhibits apoptosis of gastric cancer cells.