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 ·
   132   133   134   135   136   137   138   139   140