https://commons.ru.ac.za/vital/access/manager/Index ${session.getAttribute("locale")} 5 Synthesis, characterisation and evaluation of ferrocene-containing Novobiocin analogues for anticancer and antiplasmodial activity through inhibition of Hsp90 https://commons.ru.ac.za/vital/access/manager/Repository/vital:28690 Wed 19 Apr 2023 13:28:11 SAST ]]> Towards a biological profile for South African perinatal remains: osteological and genetic perspectives https://commons.ru.ac.za/vital/access/manager/Repository/vital:29198 Wed 15 Mar 2023 15:47:55 SAST ]]> Evaluating metabolism-induced toxicity using a non-hepatic cell line https://commons.ru.ac.za/vital/access/manager/Repository/vital:28087 Wed 15 Mar 2023 09:37:04 SAST ]]> Hop as an anti-cancer drug target https://commons.ru.ac.za/vital/access/manager/Repository/vital:41156 Wed 12 May 2021 14:04:32 SAST ]]> Repurposing a polymer precursor scaffold for medicinal application: Synthesis, characterization and biological evaluation of ferrocenyl 1,3-benzoxazine derivatives as potential antiprotozoal and anticancer agents https://commons.ru.ac.za/vital/access/manager/Repository/vital:41124 Wed 01 Dec 2021 08:13:26 SAST ]]> The Role of HSP70/HSP90 Organizing Protein (Hop) in the Heat Shock Factor 1 (HSF1)-mediated Stress Response https://commons.ru.ac.za/vital/access/manager/Repository/vital:41018 Tue 30 Nov 2021 08:34:14 SAST ]]> Establishment of human OCT4 as a putative HSP90 client protein: a case for HSP90 chaperoning pluripotency https://commons.ru.ac.za/vital/access/manager/Repository/vital:45415 Tue 25 Apr 2023 09:58:18 SAST ]]> Investigating the role of Hsp90 and LRP1 in FN matrix dynamics https://commons.ru.ac.za/vital/access/manager/Repository/vital:20319 Thu 16 Mar 2023 12:59:53 SAST ]]> The Role of HOP in Emerin-Mediated Nuclear Structure https://commons.ru.ac.za/vital/access/manager/Repository/vital:27485 Thu 13 Apr 2023 12:46:26 SAST ]]> Fucoidans from South African brown seaweeds: establishing the link between their structure and biological properties (anti-diabetic and anti-cancer activities) https://commons.ru.ac.za/vital/access/manager/Repository/vital:65775 100 kDa through ultracentrifugation. Mass spectrometry also detected the most abundant peak for all fucoidans to be around 700 Da (m/z). Extracted fucoidans inhibited the activity of α-glucosidase more strongly than the commercial anti-diabetic agent acarbose but were inactive on α-amylase. Fucoidans were also shown to be mixed inhibitors of α-glucosidase. Compellingly, fucoidans synergistically inhibited α-glucosidase in combination with the anti-diabetic agent acarbose, highlighting prospects for combination therapy. Finally, fucoidans demonstrated some anti-proliferative characteristics on HCT116 cancer cells by inhibiting their ability to adhere to the tissue culture plate matrix. Furthermore, some fucoidan extracts inhibited the migration of HCT116 cancer cells from 3D spheroids. Some of our fucoidan extracts also inhibited HCT116 colony formation, demonstrating inhibition of long-term cell survival. The E. maxima water extract also inhibited glucose uptake by HCT116 cells, thereby influencing the glycolytic flux. In conclusion, biologically active fucoidans were successfully extracted from South African brown seaweeds. These fucoidans demonstrated anti-diabetic and anti-cancer properties, revealing their relevance as potential drugs for these diseases.]]> Thu 11 Jan 2024 18:08:05 SAST ]]> The role of Stress Inducible Protein 1 (STI1) in the regulation of actin dynamics https://commons.ru.ac.za/vital/access/manager/Repository/vital:45409 Mon 24 Apr 2023 15:12:54 SAST ]]> The effects of extracellular and intracellular Hop on cell migration processes https://commons.ru.ac.za/vital/access/manager/Repository/vital:45410 Mon 24 Apr 2023 11:43:19 SAST ]]>