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Chemical structure of emodin azide methyl anthraquinone derivative.

Chemical structure of emodin azide methyl anthraquinone derivative.

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Many anticancer active compounds are known to have the capacity to destroy pathologically proliferating cancer cells in the body, as well as to destroy rapidly proliferating normal cells. Despite remarkable advances in cancer research over the past few decades, the inclusion of natural compounds in researches as potential drug candidates is becomin...

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... These are capable of self-renewal and differentiation into different populations of tumour cells, leading to tumour growth, metastasis, tumour recurrence and resistance to therapies (52)(53)(54)(55). As a result, the present study examined the expression of two putative CSC markers, CD44 and EpCAM, in patients with HCC (56)(57)(58)(59)(60). At the cut off value of >5% of tumour cells with staining, 40 and 33% of the cases were CD44-positive and EpCAM-positive, respectively. ...
... More recently, emodin, which is a natural product found in the roots of a number of plants and an anthraquinone derivate, has been shown to inhibit the proliferation of CD44-positive tumour cells. Further research should investigate whether the antitumour activity of emodin in HCC cells is accompanied by increased toxicity (60,61). While none of the patients in the present study exhibited nuclear staining of CD44, 7% of the cases exhibited nuclear expression of EpCAM, and the nuclear expression of EpCAM was associated with poor prognosis (25.67 vs. 53.52 ...
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... Inhibit the growth of HCC cells and inhibiting cell proliferation Induce apoptosis and inhibit tumor cell migration and invasion. 134 cascades and genetic changes that lead to HCC, as well as the connection between liver cirrhosis, dysplastic nodules, and HCC, can lead to better ways for preventing and treating the illness. Better patient outcomes can be achieved through the examination, diagnosis, and treatment of HCC if healthcare providers from different fields work together. ...
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... Emodin repressed the growth of human lung epithelial (A549) cells in BALB/c nude mice by inducing ER stress-dependent apoptosis. Emodin increased TRIB3/ER stress signaling and nuclear factor-B signaling, according to the in vitro molecular mechanism [139]. Likewise, Genistein, a naturally occurring isoflavone with properties resembling estrogen, can be found in soybeans. ...
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... Intestinal discomfort and severe diarrhea brought on by an overdose of emodin due to its laxative properties lead to an electrolyte imbalance and dehydration [179]. Generally, it is also known to have kidney toxicity, hepatotoxicity, and reproductive toxicity, especially at high doses and long-term use [180] The extremely low bioavailability of emodin further limits its use in therapeutic applications [179]. ...
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... Intestinal discomfort and severe diarrhea brought on by an overdose of emodin due to its laxative properties lead to an electrolyte imbalance and dehydration [179]. Generally, it is also known to have kidney toxicity, hepatotoxicity, and reproductive toxicity, especially at high doses and long-term use [180] The extremely low bioavailability of emodin further limits its use in therapeutic applications [179]. ...
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... In PM, emodin and its derivatives (emodin-8-O-β-D-glucoside, aloe-emodin), chrysophanol, physcion and its glucoside-driven (physcion-8-O-β-D-glucoside), and rhein play an important role in cancer apoptosis [57]. Emodin was the most studied for cancer treatment among others, and it induced apoptosis in various cancer cell types and animal models via different pathways (Table 6) [6,60,61]. Anticancer mechanisms of action of emodin were proposed to be direct/indirect, targeting mitochondria to induce apoptosis, and regulating the signaling pathway to repress tumor migration, invasion, metastasis, and angiogenesis such as GF-β signaling [62][63][64]; Wnt/β-catenin and VEGFR2-AKT-ERK1/2 signaling [65,66], upregulating miR-34a (tumor-suppressing miR) expression, suppressing AKT, ERK1/2, SMAD2, and SMAD4, or upregulating PI3K/Akt signaling pathways [61,67]. Recently, several groups tried to incorporate emodin with nanoparticles to enhance anticancer activity [68,69]. ...
... Recently, several groups tried to incorporate emodin with nanoparticles to enhance anticancer activity [68,69]. Importantly, the versatile function of emodin in cancer treatment in vitro and in vivo has been summarized in different papers [60,62]. Some other derivatives of emodin also play an important role in anticancer, of which some of the derivatives were generated by modifying emodin structure [69], or added amino acid sequences to emodin [70], or isolating new emodin-related compounds such as β-DHA-emodin [71] and aloe-emodin [72]. ...
... Emodin could also make HL-60/ADR cells more sensitive to multiple drug resistance [24]. When combined with Azidothymidine, Emodin had an inhibitory effect on the proliferation of the K562/ ADM cells [25], Additionally, emodin is capable of treating 5-FU-resistant breast cancer [26,27]. ...