However, the trend in Fe3O4Au x Ag y NPs concept is to deliver the drugs such as anticancer and at the same time, to observe what happens to the cancerous cells without damaging the healthy cell.
Clinical trials involving telomerase inhibitors require careful consideration compared to those looking at conventional anticancer cytotoxic drugs.
The study aimed at evaluating anticancer activities, toxicity, and pharmacological activities of the curcumin compound (CUR), the crude ethanolic extracts of rhizomes of Zingiber officinale Roscoe (Ginger: ZO) and Atractylodes lancea thung.
Among the synthesized compounds, two compounds were granted NSC code and screened at National Cancer Institute (NCI -USA for aNCI -USAr activity at a single high dose (10−5 M) and fore dose in full NCI 60 cell panticancer
Among the synthesize compounds, seventeen compounds were granted NSC code and screened at National Cancer Institute (NCI), USA for anticancer activity at a single high dose (10−5 M) in full NCI 60 cell panel.
In the present study, we primarily aimed at increasing the anticancer property of GEN towards FR-α-overexpressed HeLa cellscal cancer cells by encapsulating in FA-conjugated chitosan nanoparticles.
For each entry of NPCARE, also hyperlinked is the original scientific paper or the open resource at which the anticancer activity was reported.
Herein, this study aimed at assessing the anticancer properties of compounds inhibiting FZD7 activity by disrupting its binding with the cytosolic Dishevelled (DVL) adaptator.
In the present study, we primarily aimed at increasing the anticancer property of GEN towards FR-α overexpressed HeLa cervical cancer cells by encapsulating in FA-conjugated chitosan nanoparticles (Fig. 1).
With the aforesaid background necessitating research in newer breast cancer drugs, the present work is aimed at assessing the anticancer potential of plant-mediated silver nanoparticles in vitro, against human breast cancer cell lines MCF-7.
