Marthe Chehade

Dr. Marthe Chehade


Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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9 July 2021 in Cancers
Verified
Journal Article
Open access
PDF file
AWAYANTHI WIJEWARDENE
AYANTHI WIJEWARDENE
MCMarthe Chehade
Marthe Chehade
MGMatti Gild
Matti Gild
RCRoderick Clifton-Bligh
Roderick Clifton-Bligh
Martyn BullockMartyn Bullock
Martyn Bullock
Liquid biopsies are a novel technique to assess for either circulating tumor cells (CTC) or circulating tumor DNA (ctDNA and microRNA (miRNA)) in peripheral blood samples of cancer patients. The diagnostic role of liquid biopsy in oncology has expanded in recent years, particularly in lung, colorectal and breast cancer. In thyroid cancer, the role of liquid biopsy in either diagnosis or prognosis is beginning to translate from the lab to the clinic. In this review, we describe the evolution of liquid biopsies in detecting CTC, ctDNA and miRNA in thyroid cancer patients, together with its limitations and future directions in clinical practice.

6 August 2020 in Cancers
Verified
Journal Article
Open access
PDF file
MCMarthe Chehade
Marthe Chehade
Martyn BullockMartyn Bullock
Martyn Bullock
AGAnthony Glover
Anthony Glover
Gyorgy HutvagnerGyorgy Hutvagner
Gyorgy Hutvagner
SSStan Sidhu
Stan Sidhu
Adrenocortical Carcinoma (ACC) is a rare but aggressive malignancy with poor prognosis and limited response to available systemic therapies. Although complete surgical resection gives the best chance for long-term survival, ACC has a two-year recurrence rate of 50%, which poses a therapeutic challenge. High throughput analyses focused on characterizing the molecular signature of ACC have revealed specific micro-RNAs (miRNAs) that are associated with aggressive tumor phenotypes. MiRNAs are small non-coding RNA molecules that regulate gene expression by inhibiting mRNA translation or degrading mRNA transcripts and have been generally implicated in carcinogenesis. This review summarizes the current insights into dysregulated miRNAs in ACC tumorigenesis, their known functions, and specific targetomes. In addition, we explore the possibility of particular miRNAs to be exploited as clinical biomarkers in ACC and as potential therapeutics.