US2011318834A1PendingUtilityA1
Multiple-tumor aberrant growth genes
Est. expiryFeb 17, 2015(expired)· nominal 20-yr term from priority
Inventors:Jorn BullerdiekWillem Jan Van De VenHenricus Franciscus Petrus Maria SchoenmakersRafael Mols
C12Q 2600/158A61K 38/00C12Q 1/6841A61P 9/10C07K 14/705A61P 35/02A61P 31/00C12Q 2600/112C12Q 2600/156C07K 14/4702C12Q 1/6886A61P 35/00A61P 43/00C07K 14/47C12N 15/11A61K 38/17
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Claims
Abstract
The invention relates to the multi-tumor aberrant growth gene having the nucleotide sequence of any one of the strands of any one of the members of the High Mobility Group protein genes or LIM protein genes, including modified versions and derivatives thereof. The gene and its derivatives may be used in various diagnostic and therapeutic applications.
Claims
exact text as granted — not AI-modified1 . A method for treating cells having a non-physiological proliferative capacity or macromolecules derived therefrom comprising contacting the cells or macromolecules with a nucleic acid substantially corresponding to or complementary to the HMGI-C gene, a derivative of the gene or a modulator of expression of the gene.
2 . The method as claimed in claim 1 , further comprising a method for treating cells having a non-physiological proliferative capacity and including the step of contacting said cells with a nucleic acid substantially corresponding to or complementary to the HMGI-C gene, a derivative of the gene, or a modulator of expression of the gene.
3 . The method as claimed in claim 1 , wherein said nucleic acid comprises a derivative of a multi-tumor aberrant growth gene, wherein the derivative is a nucleic acid substantially corresponding to a truncated version of the HMGI-C gene selected from the group consisting of:
a) exons 1, 2 and 3 and truncated in intron 3 after nucleotide sequence TAGGAAATGG (SEQ ID NO: 103); b) exons 1, 2, 3 and 4 and truncated in intron 4 after nucleotide sequence GCCTGCTCAG (SEQ ID NO: 134); and c) a complete coding sequence of HMGI-C and truncated in the 3′ untranslated region after one of the sequences:
TATCCTTTCA
(SEQ ID NO: 135)
TCTTTCCACT
(SEQ ID NO: 136)
ATACCACTTA
(SEQ ID NO: 137)
TTGCCATGGT
(SEQ ID NO: 138)
CACTTTCATC
(SEQ ID NO: 139)
ATAAGGACTA
(SEQ ID NO: 140)
NCTTGTNAGC.
(SEQ ID NO: 141)
4 . A macromolecule for incorporation in a therapeutic composition for cancer treatment, comprising a derivative of a multi-tumor aberrant growth gene, wherein the derivative is a nucleic acid substantially corresponding to a truncated version of the HMGI-C gene selected from the group consisting of:
a) exons 1, 2 and 3 and truncated in intron 3 after nucleotide sequence TAGGAAATGG (SEQ ID NO: 103); b) exons 1, 2, 3 and 4 and truncated in intron 4 after nucleotide sequence GCCTGCTCAG (SEQ ID NO: 134); and c) a complete coding sequence of HMGI-C and truncated in the 3′ untranslated region after one of the sequences:
TATCCTTTCA
(SEQ ID NO: 135)
TCTTTCCACT
(SEQ ID NO: 136)
ATACCACTTA
(SEQ ID NO: 137)
TTGCCATGGT
(SEQ ID NO: 138)
CACTTTCATC
(SEQ ID NO: 139)
ATAAGGACTA
(SEQ ID NO: 140)
NCTTGTNAGC.
(SEQ ID NO: 141)
5 . The macromolecule as claimed in claim 4 , wherein the derivative comprises a hybrid of the truncated version of the HMGI-C gene and its translocation partner, and the 5′ end of the translocation partner is identifiable by one of a sequence selected from the group consisting of SEQ ID NOs: 104-133 and 142-159.
6 . The method as claimed in claim 1 , wherein the complementary nucleic acid is an anti-sense molecule.Join the waitlist — get patent alerts
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