Grant Details
Grant Number: |
5R21CA206904-03 Interpret this number |
Primary Investigator: |
Chang, Hsueh-Chia |
Organization: |
University Of Notre Dame |
Project Title: |
A Solid-State Nanopore Mirna Quantification Technology |
Fiscal Year: |
2018 |
Abstract
ABSTRACT
Micro-RNAs are key gene expression regulators with great potential as biomarkers for
cancer diagnosis, prognosis, and therapeutics. There is a great demand for accurate
miRNA profiling in cancer research and in the clinics in the near future. However, the
current technologies cannot perform this very challenging task with precision, ease, low
cost, and high throughput. All main detection technologies, real-time reverse transcription
PCR (qPCR), microarray hybridization, and next-generation sequencing (NGS) face
challenges in mRNA profiling. Since
different detection technologies, protocols and
miRNA extraction and purification methods can lead to different results, interpretation of
differential expression data and comparisons across different studies is tenuous. A
technology capable of counting individual molecules of native miRNA in a complex sample
would be much preferred.
The overarching goal of this research is to develop a novel set of solid-state polymeric
nanopore technologies for fast (1 hour), sensitive (100 molecules/sample) and quantitative
measurement of a small set of miRNAs differentially expressed in cancer patients. This
proposal will focus on its preliminary development and testing with non-clinical samples.
Raw biological samples will be loaded in an integrated platform, which will perform sample
cleanup and miRNA extraction and detection all in one-chip, for minimization of sample
loss and protocol-dependent biases.
In Specific Aim 1, we will combine multi- and single- pore solid-state technologies with
dielectric thin film nanopore coatings and a newly discovered nanopore Ohmic heating
phenomenon, to develop a miRNA “capture, release and count” strategy for concentration
of a specific miRNA from a complex sample. In Specific Aim 2, we will integrate nanopore
and ionic-membrane technologies into a platform for rapid detection of a small panel of
miRNAS in raw cell-culture and/or tissue lysate samples. This design will then be
expanded to oral cancer- related miRNAs by integrating several nanopore units in a
multitarget detection platform. In Specific Aim 3 we will compare results of miRNA
measurements in cell culture and/or tissue lysate using different sample preparation
methods (the ionic-membrane chip of SA3a, and commercially available kits for miRNA
extraction) in conjunction with the proposed nanopore platform and other reference
methods (qPCR and NGS).
Our long-term goal is to develop a robust, low cost, portable multi-disease profiling
platform, capable of accurately quantifying a large miRNAs in complex samples, for
research and clinical applications in cancer. Such platform would significantly speed up
the process from biomarker discovery, validation, and regulatory approval, to translation
into clinical setting.
Publications
Conformal single cell hydrogel coating with electrically induced tip streaming of an AC cone.
Authors: Pan Z.
, Bui L.
, Yadav V.
, Fan F.
, Chang H.C.
, Hanjaya-Putra D.
.
Source: Biomaterials science, 2021-05-04; 9(9), p. 3284-3292.
PMID: 33949367
Related Citations
Liquid biopsy technologies based on membrane microfluidics: High-yield purification and selective quantification of biomarkers in nanocarriers.
Authors: Wang C.
, Senapati S.
, Chang H.C.
.
Source: Electrophoresis, 2020 Nov; 41(21-22), p. 1878-1892.
EPub date: 2020-04-09.
PMID: 32180242
Related Citations
Resistive amplitude fingerprints during translocation of linear molecules through charged solid-state nanopores.
Authors: Sensale S.
, Wang C.
, Chang H.C.
.
Source: The Journal of chemical physics, 2020-07-21; 153(3), p. 035102.
PMID: 32716192
Related Citations
A bifurcated continuous field-flow fractionation (BCFFF) chip for high-yield and high-throughput nucleic acid extraction and purification.
Authors: Zhang C.
, Sun G.
, Senapati S.
, Chang H.C.
.
Source: Lab on a chip, 2019-11-21; 19(22), p. 3853-3861.
EPub date: 2019-10-17.
PMID: 31621762
Related Citations
Acceleration of DNA melting kinetics using alternating electric fields.
Authors: Sensale S.
, Peng Z.
, Chang H.C.
.
Source: The Journal of chemical physics, 2018-08-28; 149(8), p. 085102.
PMID: 30193482
Related Citations
Simultaneous isolation and preconcentration of exosomes by ion concentration polarization.
Authors: Marczak S.
, Richards K.
, Ramshani Z.
, Smith E.
, Senapati S.
, Hill R.
, Go D.B.
, Chang H.C.
.
Source: Electrophoresis, 2018-02-27; , .
EPub date: 2018-02-27.
PMID: 29484678
Related Citations
Universal Scaling of Robust Thermal Hot Spot and Ionic Current Enhancement by Focused Ohmic Heating in a Conic Nanopore.
Authors: Pan Z.
, Wang C.
, Li M.
, Chang H.C.
.
Source: Physical review letters, 2016-09-23; 117(13), p. 134301.
EPub date: 2016-09-21.
PMID: 27715110
Related Citations
Current Technologies and Recent Developments for Screening of HPV-Associated Cervical and Oropharyngeal Cancers.
Authors: Shah S.S.
, Senapati S.
, Klacsmann F.
, Miller D.L.
, Johnson J.J.
, Chang H.C.
, Stack M.S.
.
Source: Cancers, 2016-09-09; 8(9), .
EPub date: 2016-09-09.
PMID: 27618102
Related Citations