Extracellular Vesicle Proteome of Breast Cancer Patients with and Without Cognitive Impairment Following Anthracycline-based Chemotherapy: An Exploratory Study.
Yong Qin KohDing Quan NgChiu Chin NgAdrian BoeyMeng WeiSiu Kwan SzeHan Kiat HoMunjal AcharyaCharles L LimoliAlexandre ChanPublished in: Biomarker insights (2021)
Cognitive impairment due to cancer and its therapy is a major concern among cancer patients and survivors. Extracellular vesicle (EVs) composition altered by cancer and chemotherapy may affect neurological processes such as neuroplasticity, potentially impacting the cognitive abilities of cancer patients and survivors. We investigated the EV proteome of breast cancer patients with and without cognitive impairment following anthracycline-based chemotherapy from longitudinally collected plasma. EVs were cup-shaped and positive for Flotillin-1 and TSG-101. We identified 517 differentially expressed EV proteins between the cognitive impaired and non-impaired groups during and post-chemotherapy. The observed decreased expression of p2X purinoceptor, cofilin-1, ADAM 10, and dynamin-1 in the plasma EVs of the cognitive impaired group may suggest alterations in the mechanisms underlying synaptic plasticity. The reduced expression of tight junction proteins among cognitive-impaired patients may imply weakening of the blood-brain barrier. These EV protein signatures may serve as a fingerprint that underscores the mechanisms underlying cognitive impairment in cancer patients and survivors.
Keyphrases
- cognitive impairment
- locally advanced
- poor prognosis
- papillary thyroid
- young adults
- end stage renal disease
- chronic kidney disease
- squamous cell
- binding protein
- ejection fraction
- childhood cancer
- newly diagnosed
- chemotherapy induced
- gene expression
- peritoneal dialysis
- squamous cell carcinoma
- radiation therapy
- long non coding rna
- mass spectrometry
- patient reported outcomes
- genome wide
- atomic force microscopy
- bone marrow
- subarachnoid hemorrhage
- single molecule