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Methods of diagnosing and treating fibrosis

a fibrosis and fibroblast technology, applied in the field of fibrosis diagnosis and treatment, can solve the problems of fibroblast activation, fibroblast activation remains poorly understood, and the precise molecular mechanisms underlying persistent fibroblast activation remain poorly understood, so as to facilitate the development of early diagnostic markers and prevent or reduce disease progression

Inactive Publication Date: 2016-01-28
UNIVERSITY OF ROCHESTER
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The patent text discusses what pulmonary fibrosis is and how it affects millions of people worldwide. The invention provides information on the molecular mechanisms that cause fibrotic conditions, which can help with the development of early diagnostic markers and therapeutic agents that can prevent or reduce the progression of the disease.

Problems solved by technology

This lethal lung disorder presents a major clinical challenge, since effective therapeutic agents for reversing lung fibrosis have not yet been discovered (Phan et al., “The Myofibroblast as an Inflammatory Cell in Pulmonary Fibrosis,”Curr. Top. Pathol. 93:173-82 (1999)).
However, the precise molecular mechanisms underlying persistent fibroblast activation remains poorly understood.
However, very little is known about the expression or function of YY1 in fibrotic conditions or disorders, such as lung fibrosis.

Method used

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  • Methods of diagnosing and treating fibrosis
  • Methods of diagnosing and treating fibrosis
  • Methods of diagnosing and treating fibrosis

Examples

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example 1

Animals and Silica or Bleomycin Administration

[0144]YY1 heterozygotes (YY1+ / −) and conditional knockout YY1 (YY1f / f) mice were obtained from Dr. Yang Shi (Harvard University, Boston, Mass.). All animals were grouped according to age (6-12) or weight (20-35 g). YY1+ / − mice were on a C57BL / 6 background (≧6 generations). YY1f / f mice were on a C57BL / 6 background (4 generations). These mice received 200-300 μg of silica or three units of bleomycin per kg of body weight by intratracheal injection. The background of YY1cc10 is F4 C57BL / 6. All animals were housed under specific pathogen-free conditions at the NIH in an American Association for the Accreditation of Laboratory Animal Care-approved facility. The URMC animal care and use committee approved all experimental procedures.

example 2

Construction of Clara Cell Promoter Driven YY1 (YY1cc10)

[0145]CC-10-driven YY1)(YY1CC10) mice were generated as follows. The plasmid of a rat cc10 promoter (kind gift of Dr. Z. Zhou, Johns Hopkins University) was digested with Xbal-BamHI and the DNA ends were blunted. The murine YY1 gene was digested with BamHI and the DNA ends were blunted. A YY1 insert was subcloned into a blunted rat cc10 plasmid and the plasmid was digested with HindIII and KpnI. The 4 Kb fragment was obtained and injected into zygotes of BJ6 strain to create transgenic mice. Three lines were generated and genotyping was performed using the forward primer 5′-ACTGCCCATTGCCCAAACAC (SEQ ID NO:7) and the reverse primer 5′-GATGGTCTCCACCTCGATCTCATG (SEQ ID NO:8).

example 3

Cell Lines and Isolation of Primary Mouse Lung Fibroblasts

[0146]WI-38 cells (human fetal lung fibroblasts), MLg2908 cells (mouse lung fibroblasts), LL97A cells (human adult lung fibroblasts obtained from a patient with idiopathic pulmonary fibrosis), and MRC-5 (secondary human lung fibroblasts) were all purchased from the American Type Culture Collection. 293FT cells were obtained from Invitrogen. Primary mouse lung fibroblasts were isolated as described in Baglole et al., “Isolation and Phenotypic Characterization of Lung Fibroblasts,”Meth. Mol. Med. 117:115-27 (2005), which is hereby incorporated by reference in its entirety. Briefly, lungs were minced and digested with collagenase and DNase at 37° C. for two hours. After washing with HBSS, isolated cells were collected by centrifugation and plated in T75 flasks in DMEM / F12 (1:1) containing 10% FBS and antibiotics. This was completed in a humidified atmosphere consisting of 5% CO2 and 95% air overnight. Non-adherent cells were rem...

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Abstract

The present invention is directed to methods of diagnosing and treating a fibrotic condition in a mammalian subject. These methods involve measuring the levels of trimethylation at lysine residue 27 of histone-3 and / or measuring the expression levels of EZH2 or YY-1. Agents useful for treating fibrosis or a fibrotic condition are also disclosed.

Description

[0001]This application is a division of U.S. patent application Ser. No. 13 / 126,875, filed Jul. 25, 2011, which is a U.S. national stage application under 35 U.S.C. §371 of PCT Application No. PCT / US2009 / 063016, filed Nov. 2, 2009, which claims the benefit of U.S. Provisional Patent Application Ser. No. 61 / 110,267, filed Oct. 31, 2008, which is hereby incorporated by reference in its entirety.[0002]This invention was made with government support under grant number R01 HL073952 awarded by the National Institutes of Health. The government has certain rights in this invention.FIELD OF THE INVENTION[0003]The present invention is directed to methods of diagnosing and treating a fibrotic condition in a mammalian subject.BACKGROUND OF THE INVENTION[0004]Idiopathic pulmonary fibrosis (IPF) is a progressive, chronic interstitial lung disease associated with high mortality (median survival of newly diagnosed patients is ˜3 years) and a uniformly poor prognosis (Khalil et al., “Idiopathic Pulm...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): G01N33/68A61K31/713A61K38/44C12Q1/68
CPCG01N33/6875C12Q1/6883A61K38/44A61K31/713C12Y114/11027C12Q2600/154C12Q2600/112G01N2800/52G01N2800/10C12Q2600/136C12Q2600/106C12Q2600/158A61K31/7088A61P19/04A61K45/00A61K39/395A61K39/39533A61K39/39583
Inventor GUO, JIALIN, XINGEORAS, STEVESIME, PATRICIA
Owner UNIVERSITY OF ROCHESTER
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