The Role of microRNAs in Alzheimer’s Disease and Their Therapeutic Potentials

G C A T T A C G G C A T genes Review The Role of microRNAs in Alzheimer’s Disease and Their Therapeutic Potentials Munvar Miya Shaik 1 , Ian A. Tamargo 2 , Murtala B. Abubakar 3 ID , Mohammad A. Kamal 4 ID , Nigel H. Greig 2 and Siew Hua Gan 5, * ID 1 2 3 4 5 * School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian 16150, Malaysia; Drug Design and Development Section, Translational Gerontology Branch, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA; (I.A.T.); (N.H.G.) Department of Physiology, Faculty of Basic Medical Sciences, College of Health Sciences, Usmanu Danfodiyo University, PMB 2254 Sokoto, Nigeria; Metabolomics and Enzymology Unit, Fundamental and Applied Biology Group, King Fahd Medical Research Center, King Abdulaziz University, P.O. Box 80216, Jeddah 21589, Saudi Arabia; School of Pharmacy, Monash University Malaysia, Jalan Lagoon Selatan, Bandar Sunway 47500, Selangor, Malaysia Correspondence: ; Tel.: +60-3-55144918



 Received: 8 January 2018; Accepted: 5 March 2018; Published: 21 March 2018 Abstract: MicroRNAs (miRNAs) are short, endogenous, non-coding RNAs that post-transcriptionally regulate gene expression by base pairing with mRNA targets. Altered miRNA expression profiles have been observed in several diseases, including neurodegeneration. Multiple studies have reported altered expressions of miRNAs in the brains of individuals with Alzheimer’s disease (AD) as compared to those of healthy elderly adults. Some of the miRNAs found to be dysregulated in AD have been reported to correlate with neuropathological changes, including plaque and tangle accumulation, as well as altered expressions of species that are known to be involved in AD pathology. To examine the potentially pathogenic functions of several dysregulated miRNAs in AD, we review the current literature with a focus on the activities of ten miRNAs in biological pathways involved in AD pathogenesis. Comprehensive understandings of the expression profiles and activities of these miRNAs will illuminate their roles as potential therapeutic targets in AD brain and may lead to the discovery of breakthrough treatment strategies for AD. Keywords: miRNAs; Alzheimer’s disease; BACE1 inhibitors; γ-secretase inhibitors 1. Introduction As of 2015, 47 million people worldwide are estimated to be living with dementia, 9.9 million people are estimated to be diagnosed with dementia each year, and the global costs of the disease are estimated to be 818 billion United States dollars (USD$). Due to increasing life expectancies worldwide, the prevalence of dementia is projected to double every 20 years, meaning that 131 million people will live with dementia by the year 2050. The global costs of the disease will exceed USD$ 2 trillion by 2030. The symptoms of dementia can result from a number of neurological disorders and neurodegenerative diseases. Alzheimer’s disease (AD) is the most common cause. Recent data suggest that AD is the sole cause of dementia in 38% of all elderly patients, while combinations of AD and other forms of dementia have been estimated to be the cause in an additional 48% of elderly patients, meaning that AD pathology may be involved in approximately 86% of all the cases of Genes 2018, 9, 174; doi:10.3390/genes9040174 www.mdpi.com/journal/genes Genes 2018, 9, 174 2 of 36 dementia in the elderly [1]. A previous estimate suggested that AD is the sole cause of dementia in 60% of the demented elderly population and is involved in mixed pathology in an additional 17%, meaning AD is involved in 77% of elderly dementias [2]. Dementia caused by AD is broadly characterized by the deterioration of memory and cognition with age. As the National Institute on Aging and Alzheimer Association’s 2011 revised guidelines for the diagnosis of AD suggest, AD may be separated into three stages of disease progression: preclinical AD, mild cognitive impairment (MCI) due to AD, and dementia due to AD [3–6]. Individuals with preclinical AD manifest alterations in the levels of biomarkers that are related to AD in their blood, cerebrospinal fluid (CSF), and brain, but do not display impaired memory or cognition. Individuals with MCI due to AD have some memory loss and problems with cognition that are apparent to their closest acquaintances, but do not interfere with their day-to-day life. Finally, individuals with dementia due to AD are incapacitated due to severely impaired cognition and extensive memory loss. AD is a sporadic, multifactorial disease with a number of well-studied risk factors. Age is the most significant risk factor for the development of AD. The population of AD patients over the age of 65 has been estimated to be 96% [7,8]. After age 65, the incidence of AD doubles every five years. In fact, 11% of all people age 65 and older have AD, while 32% of all people age 85 and older have the disease [7]. Family history of AD is an important risk factor as well, though autosomal-dominant genetic mutations that guarantee the development of the disease are found in less than 1% of patients diagnosed with AD [9]. Inheritance of the ε4 polymorph of apolipoprotein E (ApoE-ε4) also greatly increases one’s risk of developing AD [10,11]. Additionally, cardiovascular stress resulting from obesity, diabetes, hypercholesterolemia, and hypertension, among other things, increases an individual’s likelihood of developing AD [12–16]. Though the precise cause or causes of AD have not been identified, many of the salient characteristics of the disease at the cellular and molecular levels have been described in detail. At the cellular level, AD is characterized by the progressive loss of neurons in the cerebral cortex, as well as several other subcortical brain areas. Reduced numbers of synapses and synaptic dysfunction are observed in affected regions, as well. The deterioration and death of neurons in affected regions leads to atrophy of the AD brain [17]. At the molecular level, AD is characterized by overproduction of the 40 and 42 amino acid isoforms of β-amyloid (Aβ1–40 and Aβ1–42 ), which form insoluble, extracellular aggregates of Aβ called amyloid plaques, and by the hyperphosphorylation and aggregation of the microtubule-associated protein tau within neurons. These insoluble, intracellular aggregates are called neurofibrillary tangles (NFTs). Neuroinflammation is also responsible for neuron and synapse loss in AD. Although amyloid plaques, NFTs, and neuroinflammation have been hypothesized to be neurotoxic and responsible for the loss of neurons and synapses in AD brain, the precise cause and sequence of AD pathogenesis remains controversial. The focus of the current article is to evaluate the presently known role of microRNAs (miRNAs) in the development and progression of AD, as miRNAs are known to regulate an extensive network of cellular programmes—dysfunction of which has been linked to a b (...truncated)