MN gene and protein
View Patent ↗Identified herein is the location of the MN protein binding site, and MN proteins/polypeptides that compete for attachment to vertebrate cells with immobilized MN protein. Such MN proteins/polypeptides prevent cell-cell adhesion and the formation of intercellular contacts. The MN protein binding site is a therapeutic target that can be blocked by organic or inorganic molecules, preferably organic molecules, more preferably proteins/polypeptides that specifically bind to that site. Therapeutic methods for inhibiting the growth of preneoplastic/neoplastic vertebrate cells that abnormally express MN protein are disclosed. Vectors are provided that encode the variable domains of MN-specific antibodies and a flexible linker polypeptide separating those domains. Further vectors are disclosed that encode a cytotoxic protein/polypeptide operatively linked to the MN gene promoter or a MN gene promoter fragment comprising the HIF-1 consensus binding sequence, and which vectors preferably further encode a cytokine. The MN gene promoter is characterized, and the binding site for a repressor of MN transcription is disclosed. Further, the hypoxia inducibility of the MN gene and the uses of such inducibility are disclosed.
1. A vector for use in selectively targeting hypoxic tumors, comprising a nucleic acid that encodes a cytotoxic protein, a cytotoxic polypeptide, a cytokine, and/or a growth factor, operatively linked to a hypoxia-inducible MN/CA 9 promoter or MN/CA 9 promoter fragment, which comprises a HIF-1 consensus binding sequence, wherein said vector, when transfected into a hypoxic vertebrate cell that abnormally expresses MN/CA IX protein, inhibits the growth of said cell;
wherein said hypoxia-inducible MN/CA 9 promoter has a nucleotide sequence selected from the group consisting of:
(a) SEQ ID NO: 144 and its complementary nucleotide sequence; and
(b) nucleotide sequences that are at least 90% homologous; to the nucleotide sequences of (a); and
wherein said hypoxia-inducible MN/CA 9 promoter fragment is a fragment of the nucleotide sequence selected from the nucleotide sequences of (a) and (b), and comprises at least a nucleotide sequence selected from the group consisting of:
(c) SEQ ID NO: 146 and its complementary nucleotide sequence; and
(d) nucleotide sequences that are 90% homologous to the nucleotide sequences of (c); and
wherein said hypoxia-inducible MN/CA 9 promoter or promoter fragment has hypoxia-inducible activity.
2. The vector according to claim 1 wherein said hypoxia-inducible MN/CA 9 promoter fragment is selected from the group consisting of SEQ ID NOS: 146 and 151.
3. The vector according to claim 1 wherein said hypoxia-inducible MN/CA 9 promoter fragment has the nucleotide sequence of SEQ ID NO: 146.
4. The vector according to claim 1 wherein said hypoxia-inducible MN/CA 9 promoter has the nucleotide sequence of SEQ ID NO: 144.
5. The vector according to claim 1 wherein said HIF-1 consensus binding sequence has a nucleotide sequence selected from the group consisting of SEQ ID NOS: 145, 147, 148, 149 and 150.
6. The vector according to claim 5 wherein said nucleotide sequence is selected from the group consisting of SEQ ID NOS: 145 and 149.
7. The vector according to claim 5 wherein said nucleotide sequence is SEQ ID NO: 145.
8. The vector of claim 1 wherein said cytotoxic protein is HSV thymidine kinase.
9. The vector according to claim 1 wherein said vector comprises a nucleic acid encoding a cytotoxic protein or cytotoxic polypeptide and a cytokine operatively linked to said MN/CA 9 promoter or MN/CA 9 promoter fragment.
10. The vector of claim 1 wherein said cytokine is interferon or interleukin-2.
11. The vector of claim 1 wherein said cell is preneoplastic or neoplastic.
12. The vector of claim 1 , wherein said cytotoxic protein or cytotoxic polypeptide is an enzyme which converts a prodrug to an active drug.
13. The vector of claim 12 , wherein said enzyme which converts a prodrug to an active drug is selected from the group consisting of cytosine deaminase, thymidine phosphorylase and cytochrome p450.
14. The vector of claim 1 wherein said growth factor is a vascular growth factor.
15. The method of claim 1 , wherein said hypoxic tumor is selected from the group consisting of tumors related to head and neck cancers, head and neck squamous cell carcinoma, uterine carcinoma, uterine cervical carcinoma, renal cancer, breast cancer, lung cancer, pancreatic cancer, soft tissue sarcoma, bladder cancer, colorectal cancer, esophageal cancer, prostate cancer, ovarian cancer, endometrial cancer, squamous cell and adenosquamous carcinomas, mesodermal tumors, neuroblastomas, retinoblastomas, sarcomas, osteosarcomas, Ewing's sarcoma, melanomas, vaginal cancer, vulval cancer, gastrointestinal cancer, urinary tract cancer, kidney cancer, non-small cell lung cancer, skin cancer, liver cancer, cervical squamous cell carcinoma, cervical adenosquamous carcinoma, cervical adenocarcinoma, cervical metaplasia, and condyloma.