Cellular genes involved in oncogenesis, products of said genes and their diagnostic and therapeutic uses
OwnerPatrizia Paterlini-Brechot, Christian Brechotinventors
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Abstract
The invention concerns the identification of cellular genes involved in oncogenesis, by insertional mutagenesis of the hepatitis B virus. Besides novel genes (including a gene of the MCM family), the invention further concerns the involvement of TRAP-150, SERCA-1, hTERT, CCT7, NMP 84p, TRKB, TRUP, ST3GalVI, and IP3R1 genes in cancerology.
Claims26
An isolated nucleic acid comprising a nucleotide sequence selected from SEQ ID Nos. 2, 12, 14, 16, 18, 27, 29, 1, 3, 4, 5, 6, 7, 8, 9, 10 and 11 or a nucleotide sequence such that it encodes one of the amino acid sequences SEQ ID Nos. 13, 15, 17, 19, 28 and 30.
An isolated nucleic acid referred to as 83T, comprising a nucleotide sequence included between nucleotides 881787 and 812959 of the supercontig NT025651.
An isolated nucleic acid referred to as FR7, comprising a nucleotide sequence included between nucleotides 2128117 and 2130561 of the supercontig NT009622.
An isolated nucleic acid comprising a nucleotide sequence located in proximity to one of the sequences SEQ ID Nos. 7 and 10.
A method of in vitro diagnosis of a tumor or of a predisposition to developing a tumor, comprising the steps consisting in:
- a1) bringing a biological sample containing DNA or RNA into contact with specific oligonucleotides allowing the amplification of all or part of a gene involved in oncogenesis or of its transcript, said gene comprising a sequence selected from SEQ ID Nos. 1, 3, 7, 9, 10, 11, 20, 24, 2, 12, 14, 16, 18, 21, 25, 27 and 29;
- b1) amplifying said DNA or RNA;
- c1) detecting the amplification products;
- d1) comparing the amplification products obtained to those obtained with a control sample, and detecting in this way a possible abnormality in said gene or in its transcript or else an abnormal number of copies of said gene, indicating a tumor or a predisposition to developing a tumor, or
- a2) bringing a biological sample containing mRNA obtained from a sample of suspect cells from a patient into contact with specific oligonucleotides allowing the amplification of all or part of the transcript of said gene, comprising a sequence selected from SEQ ID Nos. 1, 3, 7, 9, 10, 11, 20, 24, 2, 12, 14, 16, 18, 21, 25, 27 and 29;
- b2) amplifying said transcript;
- c2) detecting and quantifying the amplification products;
- a modification of the level of transcript of said gene compared to the normal control being an indicator of a tumor or of a predisposition to developing a tumor.
A method of in vitro diagnosis of a tumor or of a predisposition to developing a tumor, comprising the steps consisting in:
- a1) bringing a biological sample containing DNA or RNA into contact with specific oligonucleotides allowing the amplification of all or part of a gene involved in oncogenesis or of its transcript, said gene being selected from IP3R1, CCT7, NMP p84, TRKB, TRUP and ST3GalVI;
- b1) amplifying said DNA or RNA;
- c1) detecting the amplification products;
- d1) comparing the amplification products obtained to those obtained with a control sample, and detecting in this way a possible abnormality in said gene or in its transcript or else an abnormal number of copies of said gene, indicating a predisposition to developing a tumor, or
- a2) bringing a biological sample containing mRNA obtained from a sample of suspect cells from a patient into contact with specific oligonucleotides allowing the amplification of all or part of the transcript of said gene selected from IP3R1, CCT7, NMP p84, TRKB, TRUP and ST3GalVI;
- b2) amplifying said transcript;
- c2) detecting and quantifying the amplification products;
- the modification of the level of transcript of said gene compared to the normal control being an indicator of a tumor or of a predisposition to developing a tumor.
A method of in vitro diagnosis of a tumor or of a predisposition to developing a tumor, comprising bringing at least one antibody directed against the polypeptide comprising a sequence selected from SEQ ID Nos. 13, 15, 17, 19, 22, 26, 28 or 30 or encoded by a nucleotide sequence comprising a sequence selected from SEQ ID Nos. 1, 3, 7, 9, 10, 11, 20, 24, 2, 12, 14, 16, 18, 21, 25, 27 and 29 into contact with a biological sample, under conditions which allow the possible formation of specific immunocomplexes between said polypeptide and said antibody or antibodies, and detecting and/or quantifying the specific immunocomplexes possibly formed.
A method of in vitro diagnosis of a tumor or of a predisposition to developing a tumor, comprising bringing at least one antibody directed against a polypeptide selected from IP3R1, CCT7, NMP p84, TRKB, TRUP and ST3GalVI into contact with a biological sample, under conditions which allow the possible formation of specific immunocomplexes between said polypeptide and said antibody or antibodies, and detecting and/or quantifying the specific immunocomplexes possibly formed.
The use of a nucleic acid comprising a sequence selected from SEQ ID Nos. 1, 3, 7, 9, 10, 11, 20, 24, 2, 12, 14, 16, 18, 21, 25, 27 and 29, of an antisense of said nucleic acid, of a polypeptide encoded by said nucleic acid, or of an antibody against said polypeptide, for producing a medicinal product intended to treat tumors.
The use of a nucleic acid comprising a sequence of a gene selected from IP3R1, CCT7, NMP p84, TRKB, TRUP and ST3GalVI, of an antisense of said nucleic acid, of a polypeptide encoded by said nucleic acid, or of an antibody against said polypeptide, for producing a medicinal product intended to treat tumors.
A method of detecting genes involved in oncogenesis, comprising the steps consisting in
- extracting DNA from a tumoral liver tissue;
- amplifying, in vitro, by Alu-PCR, a nucleotide sequence at the viral DNA/cellular DNA junction;
- sequencing said nucleotide sequence,
- identifying one or more genes comprising, or located in proximity to, said sequence thus sequenced;
- characterized in that the amplification step uses a primer comprising the sequence 5′TGCCCAAGGTCTTACATAAGAGGA3′.
Dependencies are inferred from the claim text.