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Materials and Methods Related to Modulation of Mismatch Repair and Genomic Stability by miR-155

a technology of genomic stability and material and method, applied in the field of molecular biology, can solve the problems of difficult diagnosis and effective treatment of mismatched nucleotides, and the possibility of mismatches

Inactive Publication Date: 2013-03-14
THE OHIO STATES UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention is based on the discovery that inactivation of the mismatch repair (MMR) gene is the cause of the common cancer predisposition disorder Lynch Syndrome and is also involved in the development of various cancers. The invention provides compositions of matter comprising anti-sense miRNA and at least one additional composition, such as chemotherapy drugs, stem cells, or miRNA-155 inhibitors, for treating MMR dysfunction-related diseases. The invention also provides methods for diagnosing and prognosising MMR dysfunction and cancer, as well as methods for identifying MMR dysfunctional cells and treating cancer in patients with MMR dysfunction.

Problems solved by technology

Mismatched nucleotides may arise from polymerase mis-incorporation errors, recombination between heteroallelic parental chromosomes, or chemical and physical damage of the DNA.
In spite of considerable research into diseases associated with MMR dysfunction, they remain difficult to diagnose and treat effectively, and the mortality observed in patients indicates that improvements are needed in the diagnosis, treatment and prevention of these diseases.

Method used

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  • Materials and Methods Related to Modulation of Mismatch Repair and Genomic Stability by miR-155
  • Materials and Methods Related to Modulation of Mismatch Repair and Genomic Stability by miR-155
  • Materials and Methods Related to Modulation of Mismatch Repair and Genomic Stability by miR-155

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example 1

[0136]Materials and Methods Used

[0137]Cell Cultures and Transfection

[0138]Colo-320 DM, HCT-116 and DLD-1 colorectal cancer (CRC) cells (American Type Culture Collection ATCC Manassas, Va.) were cultured in RPMI 1640 (Gibco, Carlsbad, Calif.), MV4-11 B myelomonocytic leukemia cells (ATCC Manassas, Va.) and packaging cells 293TN (System Biosciences, Mountain View, Calif.) were grown in DMEM (Gibco, Carlsbad, Calif.). All cells were supplemented with 10% fetal bovine serum (Sigma, St. Louis, Mo.) plus antibiotics. Cells were checked for Mycoplasma contamination periodically and before functional experiments and were always found negative. Cells were transfected in 6-well plates by using Lipofectamine 2000 (Invitrogen, Carlsbad, Calif.) following manufacturer's protocol. For over-expression studies specific miRNA or control precursor oligonucleotides were purchased from Ambion (Austin, Tex.) and used at 100 nM. For silencing experiments miRCURY LNA™ anti-miR-155 or control miRCURY knock...

example 2

[0161]Transfections.

[0162]Colo-320 DM, HCT-116, and DLD1 cells were transfected by using Lipofectamine 2000 (Invitrogen, Carlsbad, Calif.), while MV4-11 Lentiviral vectors for miR-155 over-expression and empty vector were generated by System Biosciences (Mountain View, Calif.) according to the manufacturer's instructions. Microsatellite instability was evaluated by genotyping analysis using diagnostic primers. Genomic DNA from MSI patients was sequenced. Statistical analysis: results are expressed as mean±standard error (S.E.M), unless indicated otherwise. Comparisons between groups were performed using the two-tailed Student's t test. Significance was accepted when p was less than 0.05. Graphpad Prism v5.0 (Graphpad Software Inc.) analysis was used for the Pearson's correlation.

example 3

[0163]hMLH1, hMSH2 and hMSH6 are Targets of miR-155.

[0164]The inventors used in silico prediction models to identify potential binding sites for miR-155 in the mRNA of the core MMR genes. Two putative sites were found in hMLH1 using RNAhybrid (BiBiServ, Germany; NCBI NM—000249.2), one in the 3′-UTR and the other in the coding sequence (CDS) of (NCBI NM—000249.2); one site in the 3′-UTR of hMSH2 using TargetScan (Whitehead Institute, MIT; NCBI NM—000251.1); and one in the CDS of hMSH6 using RNAhybrid (BiBiServ, Germany; NCBI NM—000179.2) (FIG. 1A; FIG. 6).

[0165]As a functional screen the inventors subcloned the coding and 3′-regions including the predicted miR-155 seed regions of MLH1, MSH2 or MSH6 downstream of the luciferase gene and recorded Luciferase protein activity. The inventors used MMR proficient colo-320 DM CRC cells for these studies since they contain a low basal level of miR-155. The Colo-320 DM cells were transfected with the luciferase reporter constructs and with a m...

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Abstract

The present invention provides materials and methods related to modulation of mismatch and genomic stability by miR-155.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application claims the benefit of U.S. Provisional Application No. 61 / 318,042 filed Mar. 26, 2010, the entire disclosure of which is expressly incorporated herein by reference.STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH[0002]This invention was not made with government support under Grant Numbers GM080176, CA067007, CA124541 and CA135030, awarded by the National Institutes of Health. The government may have certain rights in this invention.SEQUENCE LISTING[0003]The instant application contains a Sequence Listing which has been submitted via EFS-web and is hereby incorporated by reference in its entirety. The ASCII copy, created on Mar. 21, 2011, is named 604—51754_SEQ_LIST_OSU-10126.txt, and is 5,627 bytes in size.TECHNICAL FIELD[0004]This invention relates generally to the field of molecular biology. More particularly, it concerns cancer-related technology. Certain aspects of the invention include application in diagnostics, the...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/7088C12N5/02C12N5/09A61P35/02A61K48/00C12Q1/68A61P35/00
CPCC12N15/1137C12N2310/113C12N2310/141C12N15/113C12N2310/3231A61P35/00A61P35/02
Inventor CROCE, CARLO M.VALERI, NICOLA
Owner THE OHIO STATES UNIV
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