Compositions and methods for visualizing and eliminating cancer stem cells
View Patent ↗The present invention relates generally to the field of cancer diagnosis and treatment, and more particularly to compositions and methods that may be useful for eliminating cancer cells with stem-like characteristics. The disclosed compositions and methods may also be useful for managing breast cancer, ovarian cancer, cervical cancer or endometrial (uterine) cancer with metastases; and visualizing the cancer cells in patient's body. The compositions of the instant invention include human prolactin receptor antagonist G129R.
1. A method for inhibiting growth of cancer cells in a patient, comprising administering to the patient an effective amount of a human prolactin receptor antagonist comprising the sequence of SEQ ID NO: 4 in which a glycine residue at position 129 is substituted with another amino acid;
wherein the cancer cells do not express estrogen receptor, progesterone receptor and HER2/neu; and further wherein the cancer cells are selected from the group consisting of ovarian cancer cells, uterine (endometrial) cancer cells, cervical cancer cells and breast carcinoma cells.
2. A method for inhibiting metastases of the cancer cells of claim 1 in a patient, comprising administering to the patient an effective amount of a human prolactin receptor antagonistantagonist comprising the sequence of SEQ ID NO: 4 in which a glycine residue at position 129 is substituted with another amino acid.
3. A method for decreasing the activity of aldehyde dehydrogenase 1 (ALDH1) of the cancer cells of claim 1 in a patient, comprising administering to the patient an effective amount of human prolactin receptor antagonist comprising the sequence of SEQ ID NO: 4 in which a glycine residue at position 129 is substituted with another amino acid.
4. A method for decreasing the number of cancer stem cells in the cancer cells of claim 1 in a patient, comprising administering to the patient an effective amount of a human prolactin receptor antagonist comprising the sequence of SEQ ID NO: 4 in which a glycine residue at position 129 is substituted with another amino acid.
5. The method of claim 1 , wherein the human prolactin receptor antagonist G129R is human prolactin in which a glycine residue at position 129 is substituted with arginine.
6. The method of claim 1 , 2 , 3 or 4 wherein the glycine residue at position 129 of SEQ ID NO: 4 is substituted with an amino acid selected from the group consisting of valine, leucine, isoleucine, serine, threonine, proline, tyrosine, cysteine, methionine, arginine, histidine, tryptophan, phenylalanine, lysine, asparagine, glutamine, aspartic acid and glutamic acid.
7. The method of claim 1 , 2 , 3 , or 4 , wherein the prolactin receptor antagonist is G129R.
8. The method of claim 1 , wherein the human prolactin receptor antagonist is conjugated to an agent selected from the group consisting of toxins, radioactive isotopes and fluorescent dyes.
9. The method of claim 1 , wherein the human prolactin receptor antagonist is administered simultaneously or sequentially with a chemotherapeutic agent.
10. The method of claim 1 , 2 , 3 , or 4 , wherein the human prolactin receptor antagonist is administered by a route selected from the group consisting of parenteral, subcutaneous, intraperitoneal, intravenous, intralymphatic, intrathecal, intraventricular or intrapulmonary administration.
11. The method of claim 1 , wherein the human prolactin receptor antagonist is administered subsequently to resection of cancer.