Methods and nucleic acids for the analyses of cellular proliferative disorders
The invention provides methods, nucleic acids and kits for detecting, or for detecting and distinguishing between or among liver cell proliferative disorders or for detecting, or for detecting and distinguishing between or among colorectal cell proliferative disorders. The invention discloses genomic sequences the methylation patterns of which have utility for the improved detection of and differentiation between said class of disorders, thereby enabling the improved diagnosis and treatment of patients.
1. An isolated modified DNA molecule consisting of a sequence selected from the group consisting of SEQ ID NO:2 and SEQ ID NO:3, wherein at least one cytosine base of the sequence is converted to uracil.
2. A composition comprising an isolated nucleic acid molecule or its isolated fully complementary nucleic acid molecule, and
(i) an entity selected from the group consisting of chromophores, fluorophores, lipids, cholic acid, thioethers, aliphatic chains, phospholipids, polyamines and polyethylene glycol, wherein the isolated nucleic acid molecule or the fully complementary nucleic acid molecule is chemically linked to the entity, or
(ii) a solid phase support, wherein the isolated nucleic acid molecule or the fully complementary nucleic acid molecule is bound to the solid phase support, and
wherein the isolated nucleic acid molecule or the complementary nucleic acid molecule is no more than 35 nucleotides in length, wherein the isolated nucleic acid molecule has a sequence comprising at least 16 contiguous nucleotides of a nucleic acid sequence selected from the group consisting of SEQ ID NO:2 and SEQ ID NO: 3, and wherein the 5′ cytosine bases within the at least 16 contiguous nucleotides of SEQ ID NO:2 or SEQ ID NO:3 are converted to uracil or thymine, or wherein the 5′ cytosine bases within the fully complementary nucleic acid are converted to uracil or thymine.
3. The composition of claim 2 , wherein the at least 16 contiguous nucleotides comprises at least one CpG, TpG or CpA dinucleotide sequence.
4. An isolated DNA molecule no more than 35 nucleotides in length comprising at least 16 contiguous nucleotides of a nucleic acid sequence selected from the group consisting of SEQ ID NO: 2 and SEQ ID NO: 3, wherein the at least 16 contiguous nucleotides includes at least one CpC, CpA or CpT dinucleotide(s), and wherein the 5′ cytosine bases of the at least one CpC, CpA and CpT dinucleotide(s) within the at least 16 contiguous nucleotides of SEQ ID NO:2 or SEQ ID NO:3 are converted to uracil or to thymine; or an isolated complementary DNA molecule no more than 35 nucleotides in length having a sequence fully complementary to at least 16 contiguous nucleotides of a nucleic acid sequence selected from the group consisting of SEQ ID NO:2 or SEQ ID NO:3, wherein the fully complementary sequence includes at least one CpC, CpA or CpT dinucleotide(s), and wherein the 5′ cytosine bases of the at least one CpC, CpA and CpT dinucleotide(s) within the fully complementary sequence are converted to uracil or thymine.
5. An isolated nucleic acid molecule no more than 35 nucleotides in length comprising at least 16 contiguous nucleotides of a nucleic acid sequence selected from the group consisting of SEQ ID NO: 2 and SEQ ID NO: 3, wherein the at least 16 contiguous nucleotides includes at least one CpC, CpA or CpT dinucleotide(s), and wherein the 5′ cytosine bases of the at least one CpC, CpA and CpT dinucleotide(s) within the at least 16 contiguous nucleotides of SEQ ID NO:2 or SEQ ID NO:3 are converted to uracil or to thymine; or an isolated complementary nucleic acid molecule no more than 35 nucleotides in length having a sequence fully complementary to at least 16 contiguous nucleotides of a nucleic acid sequence selected from the group consisting of SEQ ID NO:2 or SEQ ID NO:3, wherein the fully complementary sequence includes at least one CpC, CpA or CpT dinucleotide(s), and wherein the 5′ cytosine bases of the at least one CpC, CpA and CpT dinucleotide(s) within the fully complementary sequence are converted to uracil or thymine.