2022
DOI: 10.1016/j.ctrv.2022.102445
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Tailoring adjuvant endocrine therapy in early breast cancer: When, how, and how long?

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Cited by 15 publications
(7 citation statements)
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“…In addition, resistance to cisplatin in intrahepatic cholangiocarcinoma promotes the degradation of CDKN1B mRNA via YTHDF2 in an m 6 A-dependent manner ( 78 ). Tamoxifen is a conventional chemotherapy drug for breast cancer ( 79 ). Breast cancer develops tamoxifen resistance due to an increased ROS production and p38 activation.…”
Section: Amentioning
confidence: 99%
“…In addition, resistance to cisplatin in intrahepatic cholangiocarcinoma promotes the degradation of CDKN1B mRNA via YTHDF2 in an m 6 A-dependent manner ( 78 ). Tamoxifen is a conventional chemotherapy drug for breast cancer ( 79 ). Breast cancer develops tamoxifen resistance due to an increased ROS production and p38 activation.…”
Section: Amentioning
confidence: 99%
“…Endocrine therapy can be used for all patients affected by BC that express ERs and PRs—specifically, LumA, LumB and normal-like BC and as adjuvant and neoadjuvant in several types of BCs [ 42 , 43 ]. However, due to the well-known limits of this type of therapy, the search for new ER inhibitors is still ongoing [ 44 ].…”
Section: Breast Cancer Therapiesmentioning
confidence: 99%
“…Furthermore, YTHDF2 increased CDKN1B mRNA degradation in an m 6 A-dependent manner, which promoted intrahepatic cholangiocarcinoma (ICC) progression and reduced sensitivity to cisplatin treatment [121]. m 6 A modifications also play an integral part in tamoxifen resistance, a classical chemotherapeutic agent in breast cancer treatment [122]. METTL3 promoted the translation of AK4 mRNA by increasing m 6 A levels and facilitated ROS production and activation of p38, ultimately resulting in tamoxifen resistance [123].…”
Section: Induced Specific Drug Resistancementioning
confidence: 99%