Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
Add filters








Year range
1.
Journal of Southern Medical University ; (12): 544-551, 2023.
Article in Chinese | WPRIM | ID: wpr-986960

ABSTRACT

OBJECTIVE@#To analyze the expression of hydroxysteroid dehydrogenase like 2 (HSDL2) in rectal cancer tissues and the effect of changes in HSDL2 expression level on proliferation of rectal cancer cells.@*METHODS@#Clinical data and tissue samples of 90 patients with rectal cancer admitted to our hospital from January 2020 to June 2022 were collected from the prospective clinical database and biological specimen database. The expression level of HSDL2 in rectal cancer and adjacent tissues was detected by immunohistochemistry, and based on the median level of HSDL2 expression, the patients were divided into high expression group (n=45) and low expression group (n=45) for analysis the correlation between HSDL2 expression level and the clinicopathological parameters. GO and KEGG enrichment analyses were performed to explore the role of HSDL2 in rectal cancer progression. The effects of changes in HSDL2 expression levels on rectal cancer cell proliferation, cell cycle and protein expressions were investigated in SW480 cells with lentivirus-mediated HSDL2 silencing or HSDL2 overexpression using CCK-8 assay, flow cytometry and Western blotting.@*RESULTS@#The expressions of HSDL2 and Ki67 were significantly higher in rectal cancer tissues than in the adjacent tissues (P < 0.05). Spearman correlation analysis showed that the expression of HSDL2 protein was positively correlated with Ki67, CEA and CA19-9 expressions (P < 0.01). The rectal cancer patients with high HSDL2 expressions had significantly higher likelihood of having CEA ≥5 μg/L, CA19-9 ≥37 kU/L, T3-4 stage, and N2-3 stage than those with a low HSDL2 expression (P < 0.05). GO and KEGG analysis showed that HSDL2 was mainly enriched in DNA replication and cell cycle. In SW480 cells, HSDL2 overexpression significantly promoted cell proliferation, increased cell percentage in S phase, and enhanced the expression levels of CDK6 and cyclinD1 (P < 0.05), and HSDL2 silencing produced the opposite effects (P < 0.05).@*CONCLUSION@#The high expression of HSDL2 in rectal cancer participates in malignant progression of the tumor by promoting the proliferation and cell cycle progress of the cancer cells.


Subject(s)
Humans , CA-19-9 Antigen , Ki-67 Antigen/metabolism , Prospective Studies , Cell Line, Tumor , Cell Proliferation/genetics , Rectal Neoplasms/genetics , Cell Cycle , Gene Expression Regulation, Neoplastic , Hydroxysteroid Dehydrogenases/metabolism
2.
Indian J Exp Biol ; 2004 Feb; 42(2): 143-8
Article in English | IMSEAR | ID: sea-60643

ABSTRACT

Effects of lead (Pb) and cadmium (Cd) both alone or in combination on the binding of LH and FSH on isolated granulosa cells were studied. Granulosa cells isolated from proestrous rats were incubated (in vitro) with lead acetate and/or cadmium acetate (0.03 microM of Pb or Cd) for 1 hr. LH binding was dropped to 84% in Pb treated cells, 72.5% in Cd treated cells and 74.8% in combined metal treated cells compared to control. FSH binding dropped to 85.5% in Pb treated cells, 71.16% in Cd treated cells and 72.5% in combined metal treated cells compared to control. Activity of 17beta Hydroxy Steroid Dehydrogenase (17betaHSDH), a key steroidogenic enzyme was reduced by 52% in Cd and 37% in combined metal exposed cells whereas Pb exposed cells showed 31% reduction in the enzyme activity. Pretreatment with SH groups protectants (glutathione [GSH], dithiothretol [DTT]) and zinc caused an ameriolation in enzyme activity whereas Zn pretreatment showed an increase in gonadotropin binding in metal exposed cells. These results suggest that both Pb and Cd can cause a reduction in LH and FSH binding, which significantly alters steroid production in vitro and exerts a direct influence on granulosa cell function.


Subject(s)
Animals , Cadmium/toxicity , Dithiothreitol/pharmacology , Drug Combinations , Female , Follicle Stimulating Hormone/metabolism , Glutathione/pharmacology , Granulosa Cells/drug effects , Hydroxysteroid Dehydrogenases/metabolism , Lead/toxicity , Luteinizing Hormone/metabolism , Proestrus/drug effects , Rats , Steroids/biosynthesis , Zinc/pharmacology
3.
Indian J Exp Biol ; 2001 Dec; 39(12): 1249-53
Article in English | IMSEAR | ID: sea-60714

ABSTRACT

Adult male rats received daily injections (sc) of gonadotropin releasing hormone antagonist (0.2 mg/kg(-1) x day(-1)) for 21 days when they were sacrificed on day 22, adrenal weight, adrenal A5-3beta (delta 5-3beta) hydroxysteroid dehydrogenase (Delta5-3beta-HSD) activity and serum level of corticosterone were increased significantly while testicular 17beta (17beta) hydroxysteroid dehydrogenase (17beta-HSD) activity and serum level of testosterone and spermatogenesis were decreased in the rats fed on 5% casein diet. GnRH antagonist treated rats fed on 20% casein diet, resulted significant decrease in adrenal weight, serum corticosterone and adrenal A5-3beta-HSD activity while testicular 17beta-HSD activity serum testosterone levels and the weights of sex organs were increased with respect to anti GnRH treated rats fed on 5% casein diet. But the GnRH antagonist treated rats fed on 20% casein diet showed decreased spermatogenesis quantitatively and sperm count appeared similar to anti GnRH treated rats fed on 5% casein diet. These results indicate that high casein diet protects adrenocortical activity and stimulates testosterone synthesis without effecting spermatogenic arrest in GnRH antagonist treated rats. It may be concluded that GnRH antagonist in presence of high milk protein diet may be considered to be a suitable antihormone in the development of an ideal male contraceptive.


Subject(s)
Adrenal Glands/enzymology , Animals , Caseins/administration & dosage , Dietary Proteins/administration & dosage , Gonadotropin-Releasing Hormone/antagonists & inhibitors , Hydroxysteroid Dehydrogenases/metabolism , Male , Rats , Rats, Wistar , Spermatogenesis , Testis/enzymology
4.
Indian J Physiol Pharmacol ; 1994 Apr; 38(2): 141-2
Article in English | IMSEAR | ID: sea-106950

ABSTRACT

Mitomycin C (MC), an antibiotic which depresses DNA synthesis causes suppression of enzyme delta 5 3 beta-hydroxysteroid dehydrogenase (delta 5 3 beta OHD) and glucose-6 phosphate dehydrogenase (G-6 PD) in the rat adrenal tissue. The treatment resulted in a fall in DNA content together with an accumulation of cholesterol and ascorbic acid in the gland. The results suggest a diminution in adrenal steroid biogenesis similar to gonadal inhibition previously reported.


Subject(s)
11-beta-Hydroxysteroid Dehydrogenases , Adrenal Glands/drug effects , Animals , Ascorbic Acid/metabolism , Cholesterol/metabolism , DNA/metabolism , Female , Glucosephosphate Dehydrogenase/metabolism , Hydroxysteroid Dehydrogenases/metabolism , Mitomycin/pharmacology , Rats , Rats, Wistar , Steroids/biosynthesis
5.
Indian J Physiol Pharmacol ; 1983 Jan-Mar; 27(1): 7-12
Article in English | IMSEAR | ID: sea-107718

ABSTRACT

The adult Wistar strain albino rats were vasectomised by conventional method and maintained for six months. The vasectomized rat testis had elevated water content with depleted dry matter. Glycogen content was increased with indication of mobilization of hexoses into HMP pathway. The vasectomized rat testis showed preferential utilisation of triglycerides. In view of increased 3 beta-HSD and 17 beta-HSD activities, accelerated androgenesis was envisaged in vasectomized rat testis.


Subject(s)
Animals , Cholesterol/blood , Fatty Acids, Nonesterified/blood , Glycerol/blood , Hydroxysteroid Dehydrogenases/metabolism , Lipids/blood , Male , Phospholipids/blood , Rats , Rats, Inbred Strains , Testis/metabolism , Triglycerides/blood , Vasectomy
7.
Indian J Physiol Pharmacol ; 1975 Apr-Jun; 19(2): 58-64
Article in English | IMSEAR | ID: sea-106486

ABSTRACT

The activity of delta5-3beta Hydroxysteroid hydro-genase, dihydro orotic dehydrogenase, B-Hydroxybutyrate dehydrogenase and glucose-6-phosphate dehydrogenase was studied in the testes of hereditary dwarf mice treated with Prolactin or LH. Two months old dw/dw dwarf mice were injected twice daily, for 14 days, either with 100 mug ovine Prolactin, or 5 mug ovine LH twice a day. Prolactin treatment increased the activity of all the enzymes assessed. Treatment with LH stimulated the activity of all the enzymes as compared to the saline treated animals but less than the Prolactin treated ones. The data bearing that the increased activity of several oxidising enzymes in the testes of hereditary dwarf mice is increased with Prolactin, is consistent with the suggested effect of this hormone on testicular steroidogenesis.


Subject(s)
Animals , Dwarfism/enzymology , Epididymis/pathology , Glucosephosphate Dehydrogenase/metabolism , Hydroxybutyrate Dehydrogenase/metabolism , Hydroxysteroid Dehydrogenases/metabolism , Leydig Cells/enzymology , Luteinizing Hormone/pharmacology , Male , Mice , Organ Size/drug effects , Orotic Acid , Oxidoreductases/metabolism , Prolactin/pharmacology , Rodent Diseases/pathology , Seminal Vesicles/pathology , Stimulation, Chemical , Testis/enzymology
SELECTION OF CITATIONS
SEARCH DETAIL