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2 protocols using chrysin

1

Chrysin Modulates Tumor-Associated Macrophages in Xenograft Model

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All procedures involving mice were approved by the Animal Protection and Use Committee of Ruige Biotechnology (protocol code 20230615-27). Four-week-old male BALB/c-nu/nu mice were purchased from the Guangdong Medical Experimental Animal Center (Guangzhou, China) for the establishment of the xenograft model. TAMs were coinjected with A549 cancer cells (3 × 106) in a 1:3 ratio subcutaneously into the right dorsal side of the mice. The mice were randomly divided into Ctrl group, TAMs group, and TAMs + Chrysin group, with six mice in each group. Chrysin (Meilunbio, Dalian, China) was orally administered to the mice at a dose of 30 mg/kg daily [51 (link)]. The mice were observed for growth status every other day, and body weight and tumor size (calculated using the formula: 0.52 × length × width2) were measured and recorded. After three weeks of feeding, according to humane euthanasia principles, the mice were euthanized, and tissues were collected. The collected tumor tissues were fixed in 4% paraformaldehyde for 12 h, dehydrated, embedded in paraffin, and then cut into 4 μm sections for immunohistochemistry (IHC) and hematoxylin and eosin (H&E) staining experiments. Following animal welfare principles, the experiment was terminated immediately if the animals lost 20% of their body weight, developed signs of cachexia, or if tumor size exceeded 2000 mm3.
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2

Glucuronidation of Fluorogenic Probe

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The fluorogenic probe substrate N-butyl-4-(4-hydroxyphenyl)-1,8-naphthalimide (NHPN) and its O-glucuronide (NHPNG) were synthesized and purified (purity≥98%) according to the previously reported scheme [13 (link)]. Nilotinib and chrysin were from Dalian Meilun Biotech Co., Ltd. (Meilun, Dalian, China). The tissue preparations, including pooled human liver microsomes (HLM), pooled human intestine microsomes (HIM), pooled human kidney microsomes (HKM), and pooled human lung microsomes (HLuM) were purchased from Celsis Inc. (Baltimore, MD, USA). Recombinant human UGT1A1 was from BD Biosciences (Woburn, MA, USA). Stably transfected HeLa cells (named HeLa-UGT1A1 cells) were constructed as previously reported [[15] (link), [16] (link), [17] ]. The uridine diphosphate-glucuronic acid (UDPGA), polyethylene glycol hexadecyl ether (Brij 58) and anti-GAPDH antibody (G8795) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Anti-UGT1A1 antibody (ab194697) was obtained from Abcam (Cambridge, MA). The reagents for the SimpleWestern blotting system were purchased from ProteinSimple (San Jose, CA). Ultrapure water purified by Milli-Q® Integral Water Purification System (Millipore, USA) was used throughout, while LC grade methanol, acetonitrile, and formic acid were ordered from Tedia (Fairfield, USA).
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