dc.contributor.author |
Ciuhrii, Veaceslav |
|
dc.contributor.author |
Olariu, Laura |
|
dc.contributor.author |
Dumitriu, Brandusa |
|
dc.contributor.author |
Ene, Diana Manuela |
|
dc.date.accessioned |
2020-05-22T18:40:11Z |
|
dc.date.available |
2020-05-22T18:40:11Z |
|
dc.date.issued |
2015 |
|
dc.identifier.citation |
CIUHRII V., OLARIU L., DUMITRIU B., et al. Original product for prostate hyperplasia treatment; mechanisms of preclinical action. In: Arta Medica. 2015, pp.131-132. ISSN 1810-1852. |
en_US |
dc.identifier.issn |
1810-1852 |
|
dc.identifier.uri |
http://repository.usmf.md/handle/20.500.12710/9767 |
|
dc.description |
NEWTONE Laboratories, Bucharest, Romania, S.C. Biotehnos S.A., Ilfov, Romania, The Academy of Romanian Scientists, Bucureşti, Romania, Al VI-lea Congres de Urologie, Dializă şi Transplant Renal din Republica Moldova cu participare internaţională (21-23 octombrie 2015) |
en_US |
dc.description.abstract |
Adenoprosin product is based on the exploitation of certain
entomological resources, whose biological systems are analogs
with the human ones in a higher percent than other natural
sources.
This compatibility is concretized in a higher responsiveness
of cellular structures to the action of the entomological
biocomplex with an optimized design towards a particular
therapeutical target. Adenoprosin is involved in inflammatory
processes associated with static and dynamic mechanisms
of prostate hyperplasia. The „in vitro” specific action was
investigated using standardized cell lines (PWR-1E - androgenresponsive
and DU-145 - prostate adenocarcinoma metastasis;
hormone independent cells) and experimental positive
controls (dutasteride - drug involved in hormone -dependent
aberrant proliferative mechanisms induced by testosterone;
methotrexate - cell division inhibitor; dexamethasone - anti by its anti-apoptotic, anti-proliferative and anti-inflammatory biological activity, proved by methods of performant cellular
and molecular multi-parametric analysis. It was highlighted the
stop of IL6 and IL8 cytokines extracellular release in stimulating
conditions with pro-inflammatory agents (phorbol-myristateacetate-
PMA and tumor necrosis factor - TNFa). As well as,
Adenoprosin shows significant action on extracellular signaling
pathways of tumor progression and invasion, inhibiting IL6
cytokine - morbidity mediator in prostate cancer and VEGF -
responsible of the onset of angiogenesis in metastatic -process,
ffie preclinical studies revealed an optimum efficacy / toxicity
profile, remarkable in the actual tendencies of therapeutical
capitalization of natural raw materials with significant biological
efficiency and minimal side effects.
In recent years, the pathologies resulted from prostate
disorders had a rising incidence, Adenoprosin covering an
important therapeutical niche on the pharmaceutical market.
The research was conducted as part of the project ENTOMED
/ Ctr DPST 26/2013. |
en_US |
dc.description.abstract |
Produsul Adenoprosin se bazeaza pe exploatarea unor
anumite resurse entomologice ale căror sisteme biologice sunt
analoge celor umane intr-un procent ridicat fata de alte surse
naturale.
Aceasta compatibilitate este concretizata printr-o
responsivitate superioara a structurilor celulare la acţiunea
biocomplexului entomologie cu design optimizat către o
anumita tinta terapeutica. Adenoprosin intervine in procese
inflamatorii asociate cu mecanisme statice si dinamice
implicate in hiperplazia de prostata. Acţiunea specifica in
vitro a fost investigata utilizând linii celulare standardizate
(PWR-1E - androgen-responsiva si DU-145 - metastaza de
adenocarcinom de prostata, hormon independenta) si martori
pozitivi experimentali (dutasterid - medicament ce intervine in
mecanismele aberant proliferative hormon-dependente induse
de testosteron, metrotrexat - inhibitor diviziune celulara,
dexametazona - agent antiinflamator) .Efectul produsului
Adenoprosin este susţinut de activitatea biologica antiapoptotica,
antiproliferativa si antiinflamatoare demonstrate in vitro prin
metode performante de analiza multiparametrica celulara si
moleculara. S-a evidenţiat stoparea eliberării de citokine IL6 si
IL8 in condiţii de stimulare cu agenţi pro-inflamatorii (forbol
miristat acetat-PMA si factor necrotic tumoral-TNFa). De
asemenea, Adenoprosin manifesta acţiune semnificativa pe caile
de semnalizare extracelulara a progresiei si invaziei tumorale
inhibând citokina IL6 - mediator al morbidităţii in cancerul
de prostata si VEGF - factor declanşator al angiogenezei in
metastazare. Studiile preclinice au evidenţiat de asemenea, un
profil eficacitate / toxicitate optim, remarcabil in tendinţele
actuale de valorificare terapeutica a materiilor prime naturale
cu activitate biologica eficienta si efecte secundare minime.
In ultimii ani, patologiile rezultate din disfunctiile prostatei
au o incidenţa crescută, produsul Adenoprosin acoperind o nisa
terapeutica importanta in piaţa farmaceuticelor.
Cercetările s-au realizat in cadrul proiectului ENTOMED /
Ctr26 DPST/2013. |
|
dc.publisher |
Asociaţia chirurgilor “Nicolae Anestiadi” din Republica Moldova |
en_US |
dc.subject.mesh |
Prostatic hyperplasia--therapy |
en_US |
dc.subject.mesh |
Adenoprosin--drug therapy |
en_US |
dc.subject.mesh |
Prostatic hyperplasia--diagnosis |
en_US |
dc.subject.mesh |
Prostatic hyperplasia--physiopathology |
en_US |
dc.title |
Original product for prostate hyperplasia treatment; mechanisms of preclinical action |
en_US |
dc.title.alternative |
Produs original pentru tratamentul hiperplaziei de prostată; mecanisme de acţiune preclinică |
en_US |
dc.type |
Article |
en_US |