Page 137 - 《中国药房》2024年11期
P. 137
推广到更大的人群范围。这可能是影响全面评估白藜 diates the apoptosis of triple negative breast cancer cells
芦醇抗癌效果的原因之一。 by reducing POLD1 expression[J]. Front Oncol,2021,11:
4 结论与展望 569295.
[ 6 ] AGHAZ F,ASADI Z,SAJADIMAJD S,et al. Codelivery
本文通过评估多个体外和体内研究,揭示了白藜芦
of resveratrol melatonin utilizing pH responsive sericin
醇在乳腺癌治疗中的作用。白藜芦醇能够通过诱导细
based nanocarriers inhibits the proliferation of breast can‐
胞凋亡、调控自噬(诱导和抑制均有)、抑制糖酵解来削
cer cell line at the different pH[J]. Sci Rep,2023,13(1):
弱乳腺癌细胞的增殖和存活能力。白藜芦醇既可作为
11090.
抗氧化剂直接诱导乳腺癌细胞死亡,又可通过调节肿瘤
[ 7 ] MONDAL A,BENNETT L L. Resveratrol enhances the
微环境以及 MMPs、TGF-β、上皮-间质转化和相关分子
efficacy of sorafenib mediated apoptosis in human breast
途径的表达,来抑制乳腺癌细胞的生长、转移和侵袭。 cancer MCF7 cells through ROS,cell cycle inhibition,cas‐
此外,白藜芦醇可通过抑制 ATP 结合盒转运蛋白 G2 和 pase 3 and PARP cleavage[J]. Biomed Pharmacother,
核糖核酸结合蛋白的表达,以及抑制乳腺癌细胞的上 2016,84:1906-1914.
皮-间质转化并调节 Sir2 样蛋白 1 与 β-连环蛋白之间的 [ 8 ] WANG J,HUANG P,PAN X F,et al. Resveratrol re‐
相关性,来增强乳腺癌细胞对阿霉素的敏感性或逆转乳 verses TGF-β1-mediated invasion and metastasis of breast
腺癌细胞对阿霉素的耐药性;还可通过引发氧化损伤来 cancer cells via the SIRT3/AMPK/autophagy signal axis
增强乳腺癌细胞对放疗的敏感性。 [J]. Phytother Res,2023,37(1):211-230.
然而,白藜芦醇的疏水性、非选择性、光解和化学不 [ 9 ] CHENG T T,WANG C,LU Q Q,et al. Metformin inhi-
稳定性以及在角质层的低渗透性限制了其广泛应用,但 bits the tumor-promoting effect of low-dose resveratrol,
and enhances the anti-tumor activity of high-dose resvera‐
这些局限性可以通过优化递送系统来解决。白藜芦醇
trol by increasing its reducibility in triple negative breast
的另一个局限性是白藜芦醇及其不同制剂形式的临床
cancer[J]. Free Radical Bio Med,2022,180:108-120.
试验研究数量有限,这限制了研究者对其在乳腺癌患者
[10] VERA-RAMIREZ L,VODNALA S K,NINI R,et al. Au‐
体内分布、代谢和潜在副作用的了解。尽管针对白藜芦
tophagy promotes the survival of dormant breast cancer
醇在乳腺癌治疗中的作用及其机制已开展多项临床前
cells and metastatic tumour recurrence[J]. Nat Commun,
研究,但仍需要开展白藜芦醇及其不同制剂在体内的分
2018,9(1):1944.
布、代谢和毒理的临床前和临床研究,以探讨其不同制 [11] ALAYEV A,BERGER S M,KRAMER M Y,et al. The
剂的生物相容性及其对乳腺癌的有效性。 combination of rapamycin and resveratrol blocks au‐
参考文献 tophagy and induces apoptosis in breast cancer cells[J]. J
[ 1 ] 郑荣寿,陈茹,韩冰峰,等. 2022年中国恶性肿瘤流行情 Cell Biochem,2015,116(3):450-457.
况分析[J]. 中华肿瘤杂志,2024,46(3):221-231. [12] KIM N H,SUNG N J,YOUN H S,et al. Gremlin-1 acti‐
ZHENG R S,CHEN R,HAN B F,et al. Analysis on the vates Akt/STAT3 signaling,which increases the glycolysis
prevalence of malignant tumors in China in 2022[J]. Chin rate in breast cancer cells[J]. Biochem Biophys Res Com‐
J Oncol,2024,46(3):221-231. mun,2020,533(4):1378-1384.
[ 2 ] NEDELJKOVIĆ M,DAMJANOVIĆ A. Mechanisms of [13] GOMEZ L S,ZANCAN P,MARCONDES M C,et al.
chemotherapy resistance in triple-negative breast cancer: Resveratrol decreases breast cancer cell viability and glu‐
how we can rise to the challenge[J]. Cells,2019,8(9):957. cose metabolism by inhibiting 6-phosphofructo-1-kinase
[ 3 ] WU H,CHEN L,ZHU F F,et al. The cytotoxicity effect [J]. Biochimie,2013,95(6):1336-1343.
of resveratrol:cell cycle arrest and induced apoptosis of [14] HAN X,ZHAO N,ZHU W W,et al. Resveratrol atte-
breast cancer 4T1 cells[J]. Toxins (Basel),2019,11 nuates TNBC lung metastasis by down-regulating PD-1
(12):731. expression on pulmonary T cells and converting macro‐
[ 4 ] SAKAMOTO T,TANIMOTO K,EGUCHI H,et al. Res‐ phages to M1 phenotype in a murine tumor model[J]. Cell
veratrol exhibits diverse anti-cancer activities through epi‐ Immunol,2021,368:104423.
genetic regulation of E-cadherin and p21 in triple-negative [15] SICA A,MANTOVANI A. Macrophage plasticity and po‐
breast cancer cells[J]. Breast Cancer,2023,30(5): larization:in vivo veritas[J]. J Clin Invest,2012,122(3):
727-738. 787-795.
[ 5 ] LIANG Z J,WAN Y,ZHU D D,et al. Resveratrol me- [16] CHEUK I W,CHEN J,SIU M,et al. Resveratrol en‐
中国药房 2024年第35卷第11期 China Pharmacy 2024 Vol. 35 No. 11 · 1411 ·