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Updated: Jun 30, 2026

MicroRNA Based Liquid Biopsy: The Experience of the Plasma miRNA Signature Classifier MSC for Lung Cancer Screening
Published on: October 26, 2017
Circulating microRNA-155-3p levels predicts response to first line immunotherapy in patients with metastatic renal
Maryam Soleimani1, Marisa Thi2, Sajjad Janfaza3
1Division of Medical Oncology, British Columbia Cancer-Vancouver Cancer Centre, 600 West 10th Avenue, Vancouver, BC, V5Z 4E6, Canada.
Abstract:
Predictive biomarkers of response to immune checkpoint-based therapies (ICI) remain a critically unmet need in the management of advanced renal cell carcinoma (RCC). The complex interplay of the tumour microenvironment (TME) and the circulating immune response has proven to be challenging to decipher. MicroRNAs have gained increasing attention for their role in post-transcriptional gene expression regulation, particularly because they can have immunomodulatory properties. We evaluated the presence of immune-specific extracellular vesicle (EV) microRNAs in the plasma of patients with metastatic RCC (mRCC) prior to initiation of ICI. We found significantly lower levels of microRNA155-3p (miR155) in responders to ICI, when compared to non-responders. This microRNA has unique immunomodulatory properties, thus providing potential biological rationale for our findings. Our results support further work in exploring microRNAs as potential biomarkers of response to immunotherapy.
Insights
Predicting response to immune checkpoint inhibitors (ICI) in advanced renal cell carcinoma (RCC) is crucial. Lower levels of microRNA155-3p (miR155) in plasma predict better response to ICI therapy in metastatic RCC patients.
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- Predictive biomarkers for immune checkpoint inhibitor (ICI) therapy in advanced renal cell carcinoma (RCC) are needed.
- The tumor microenvironment and systemic immune responses are complex and difficult to interpret.
- MicroRNAs are key regulators of gene expression with potential immunomodulatory roles.
Purpose of the Study:
- To investigate immune-specific extracellular vesicle (EV) microRNAs in the plasma of metastatic RCC (mRCC) patients before ICI treatment.
- To identify potential microRNA biomarkers associated with response to ICI therapy.
Main Methods:
- Plasma samples were collected from mRCC patients before initiating ICI therapy.
- Extracellular vesicle (EV)-derived microRNAs were analyzed.
- Levels of specific microRNAs, including microRNA155-3p (miR155), were quantified and compared between responders and non-responders.
Main Results:
- Significantly lower levels of microRNA155-3p (miR155) were observed in patients who responded to ICI therapy compared to non-responders.
- miR155 possesses known immunomodulatory properties, offering a potential biological explanation for the observed association.
Conclusions:
- MicroRNAs, specifically miR155, show potential as predictive biomarkers for ICI therapy response in advanced RCC.
- Further research into microRNAs could enhance immunotherapy strategies for RCC patients.
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