TY - JOUR
T1 - Computational modeling and biomarker studies of pharmacological treatment of Alzheimer's disease (Review)
AU - Hassan, Mubashir
AU - Abbas, Qamar
AU - Seo, Sung Yum
AU - Shahzadi, Saba
AU - Al Ashwal, Hany
AU - Zaki, Nazar
AU - Iqbal, Zeeshan
AU - Moustafa, Ahmed A.
PY - 2018/5/22
Y1 - 2018/5/22
N2 - Alzheimer's disease (AD) is a complex and multifactorial disease. In order to understand the genetic influence in the progression of AD, and to identify novel pharmaceutical agents and their associated targets, the present study discusses computational modeling and biomarker evaluation approaches. Based on mechanistic signaling pathway approaches, various computational models, including biochemical and morphological models, are discussed to explore the strategies that may be used to target AD treatment. Different biomarkers are interpreted on the basis of morphological and functional features of amyloid ? plaques and unstable microtubule-associated tau protein, which is involved in neurodegeneration. Furthermore, imaging and cerebrospinal fluids are also considered to be key methods in the identification of novel markers for AD. In conclusion, the present study reviews various biochemical and morphological computational models and biomarkers to interpret novel targets and agonists for the treatment of AD. This review also highlights several therapeutic targets and their associated signaling pathways in AD, which may have potential to be used in the development of novel pharmacological agents for the treatment of patients with AD. Computational modeling approaches may aid the quest for the development of AD treatments with enhanced therapeutic efficacy and reduced toxicity.
AB - Alzheimer's disease (AD) is a complex and multifactorial disease. In order to understand the genetic influence in the progression of AD, and to identify novel pharmaceutical agents and their associated targets, the present study discusses computational modeling and biomarker evaluation approaches. Based on mechanistic signaling pathway approaches, various computational models, including biochemical and morphological models, are discussed to explore the strategies that may be used to target AD treatment. Different biomarkers are interpreted on the basis of morphological and functional features of amyloid ? plaques and unstable microtubule-associated tau protein, which is involved in neurodegeneration. Furthermore, imaging and cerebrospinal fluids are also considered to be key methods in the identification of novel markers for AD. In conclusion, the present study reviews various biochemical and morphological computational models and biomarkers to interpret novel targets and agonists for the treatment of AD. This review also highlights several therapeutic targets and their associated signaling pathways in AD, which may have potential to be used in the development of novel pharmacological agents for the treatment of patients with AD. Computational modeling approaches may aid the quest for the development of AD treatments with enhanced therapeutic efficacy and reduced toxicity.
UR - http://www.scopus.com/inward/record.url?scp=85047775692&partnerID=8YFLogxK
U2 - 10.3892/mmr.2018.9044
DO - 10.3892/mmr.2018.9044
M3 - Review article
C2 - 29845262
AN - SCOPUS:85047775692
SN - 1791-2997
VL - 18
SP - 639
EP - 655
JO - Molecular Medicine Reports
JF - Molecular Medicine Reports
IS - 1
ER -