Cancer has been identified as a leading cause of death worldwide, and the increasing number of cancer cases threatens to shorten the average life expectancy of people. Recently, we reported a 3-azido-3-deoxythymidine (AZT)-based amphipathic small molecule, ADG-2e that revealed a notable potency against tumor metastasis. To evaluate the anticancer potential of ADG-2e, we assessed its anticancer potency in vitro and in vivo. Anticancer screening of ADG-2e against cervical cancer cells, HeLa CCL2, and BT549 mammary gland ductal carcinoma showed significant inhibition of cancer cell proliferation. Furthermore, mechanistic investigations revealed that cancer cell death presumably proceeded through an oncosis mechanistic pathway because ADG-2e tr...
Withaferin A, which is a naturally derived steroidal lactone, has been found to prevent angiogenesis...
DNA methyltransferases (DNMTs) are important enzymes involved in epigenetic control of gene expressi...
Chemical changes performed on 1a (sirtinol) led to a series of SIRT1/2 inhibitors, in some cases mor...
International audienceBackground and Purpose Drugs targeting microtubules are commonly used for canc...
Normal cells in culture divide a certain amount of times and undergo a process termed replicative se...
The discovery and development of novel small molecules as anti-cancer agents plays an integral role ...
Cancer stem cells are a subset of cancer cells that initiate the growth of tumors. Low levels of can...
Azidothymidine (AZT), which has been extensively used as an antiviral agent in the treatment of AIDS...
Normal cells in culture divide a certain amount of times and undergo a process termed replicative se...
Cytotoxic small-molecule drugs have a major influence on the fate of antibody�drug conjugates (ADC...
2013-05-10Advanced age is a risk-factor common to most cancers. In coming years, a marked increase i...
Abstract Background The transforming growth factor β (TGFβ) and bone morphogenetic protein (BMP) sig...
The antitumor activity of 5-aza-2′-deoxycytidine (5-aza-dCyd), a nucleoside analog, was established ...
Focal adhesion kinase (FAK) is a nonreceptor kinase that is overexpressed in many types of tumors. W...
Continued androgen receptor (AR) expression and signaling is a key driver in castration-resistant pr...
Withaferin A, which is a naturally derived steroidal lactone, has been found to prevent angiogenesis...
DNA methyltransferases (DNMTs) are important enzymes involved in epigenetic control of gene expressi...
Chemical changes performed on 1a (sirtinol) led to a series of SIRT1/2 inhibitors, in some cases mor...
International audienceBackground and Purpose Drugs targeting microtubules are commonly used for canc...
Normal cells in culture divide a certain amount of times and undergo a process termed replicative se...
The discovery and development of novel small molecules as anti-cancer agents plays an integral role ...
Cancer stem cells are a subset of cancer cells that initiate the growth of tumors. Low levels of can...
Azidothymidine (AZT), which has been extensively used as an antiviral agent in the treatment of AIDS...
Normal cells in culture divide a certain amount of times and undergo a process termed replicative se...
Cytotoxic small-molecule drugs have a major influence on the fate of antibody�drug conjugates (ADC...
2013-05-10Advanced age is a risk-factor common to most cancers. In coming years, a marked increase i...
Abstract Background The transforming growth factor β (TGFβ) and bone morphogenetic protein (BMP) sig...
The antitumor activity of 5-aza-2′-deoxycytidine (5-aza-dCyd), a nucleoside analog, was established ...
Focal adhesion kinase (FAK) is a nonreceptor kinase that is overexpressed in many types of tumors. W...
Continued androgen receptor (AR) expression and signaling is a key driver in castration-resistant pr...
Withaferin A, which is a naturally derived steroidal lactone, has been found to prevent angiogenesis...
DNA methyltransferases (DNMTs) are important enzymes involved in epigenetic control of gene expressi...
Chemical changes performed on 1a (sirtinol) led to a series of SIRT1/2 inhibitors, in some cases mor...