TY - JOUR
T1 - Adenoid cystic carcinoma
T2 - Current therapy and potential therapeutic advances based on genomic profiling
AU - Chae, Young Kwang
AU - Chung, Su Yun
AU - Davis, Andrew A.
AU - Carneiro, Benedito A.
AU - Chandra, Sunandana
AU - Kaplan, Jason
AU - Kalyan, Aparna
AU - Giles, Francis J.
PY - 2015
Y1 - 2015
N2 - Adenoid cystic carcinoma (ACC) is a rare cancer with high potential for recurrence and metastasis. Efficacy of current treatment options, particularly for advanced disease, is very limited. Recent whole genome and exome sequencing has dramatically improved our understanding of ACC pathogenesis. A balanced translocation resulting in the MYB-NFIB fusion gene appears to be a fundamental signature of ACC. In addition, sequencing has identified a number of other driver genes mutated in downstream pathways common to other well-studied cancers. Overexpression of oncogenic proteins involved in cell growth, adhesion, cell cycle regulation, and angiogenesis are also present in ACC. Collectively, studies have identified genes and proteins for targeted, mechanism-based, therapies based on tumor phenotypes, as opposed to nonspecific cytotoxic agents. In addition, although few studies in ACC currently exist, immunotherapy may also hold promise. Better genetic understanding will enable treatment with novel targeted agents and initial exploration of immune-based therapies with the goal of improving outcomes for patients with ACC.
AB - Adenoid cystic carcinoma (ACC) is a rare cancer with high potential for recurrence and metastasis. Efficacy of current treatment options, particularly for advanced disease, is very limited. Recent whole genome and exome sequencing has dramatically improved our understanding of ACC pathogenesis. A balanced translocation resulting in the MYB-NFIB fusion gene appears to be a fundamental signature of ACC. In addition, sequencing has identified a number of other driver genes mutated in downstream pathways common to other well-studied cancers. Overexpression of oncogenic proteins involved in cell growth, adhesion, cell cycle regulation, and angiogenesis are also present in ACC. Collectively, studies have identified genes and proteins for targeted, mechanism-based, therapies based on tumor phenotypes, as opposed to nonspecific cytotoxic agents. In addition, although few studies in ACC currently exist, immunotherapy may also hold promise. Better genetic understanding will enable treatment with novel targeted agents and initial exploration of immune-based therapies with the goal of improving outcomes for patients with ACC.
KW - Adenoid cystic carcinoma
KW - Genetics
KW - Immunotherapy
KW - Targeted therapy
UR - http://www.scopus.com/inward/record.url?scp=84947800955&partnerID=8YFLogxK
U2 - 10.18632/oncotarget.5076
DO - 10.18632/oncotarget.5076
M3 - Article
C2 - 26359351
AN - SCOPUS:84947800955
SN - 1949-2553
VL - 6
SP - 37117
EP - 37134
JO - Oncotarget
JF - Oncotarget
IS - 35
ER -