000 | 02035 am a22002773u 4500 | ||
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042 | _adc | ||
100 | 1 | 0 |
_aBenjamin, Mercilena _eauthor _91764 |
700 | 1 | 0 |
_aMalakar, Pushkar _eauthor _91765 |
700 | 1 | 0 |
_aSinha, Rohit Anthony _eauthor _91766 |
700 | 1 | 0 |
_aNasser, Mohd Wasim _eauthor _91767 |
700 | 1 | 0 |
_aBatra, Surinder K. _eauthor _91768 |
700 | 1 | 0 |
_aSiddiqui, Jawed Akhtar _eauthor _91769 |
700 | 1 | 0 |
_aChakravarti, Bandana _eauthor _91770 |
245 | 0 | 0 | _aMolecular signaling network and therapeutic developments in breast cancer brain metastasis |
260 | _c2023-07. | ||
500 | _a/pmc/articles/PMC7613958/ | ||
500 | _a/pubmed/36536947 | ||
520 | _aBreast cancer (BC) is one of the most frequently diagnosed cancers in women worldwide. It has surpassed lung cancer as the leading cause of cancer-related death. Breast cancer brain metastasis (BCBM) is becoming a major clinical concern that is commonly associated with ER-ve and HER2+ve subtypes of BC patients. Metastatic lesions in the brain originate when the cancer cells detach from a primary breast tumor and establish metastatic lesions and infiltrate near and distant organs via systemic blood circulation by traversing the BBB. The colonization of BC cells in the brain involves a complex interplay in the tumor microenvironment (TME), metastatic cells, and brain cells like endothelial cells, microglia, and astrocytes. BCBM is a significant cause of morbidity and mortality and presents a challenge to developing successful cancer therapy. In this review, we discuss the molecular mechanism of BCBM and novel therapeutic strategies for patients with brain metastatic BC. | ||
540 | _a | ||
540 | _ahttps://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (https://creativecommons.org/licenses/by-nc-nd/4.0/). | ||
546 | _aen | ||
690 | _aArticle | ||
655 | 7 |
_aText _2local |
|
786 | 0 | _nAdv Cancer Biol Metastasis | |
856 | 4 | 1 |
_uhttp://dx.doi.org/10.1016/j.adcanc.2022.100079 _zConnect to this object online. |
999 |
_c2038 _d2038 |