Use of arsenic for cancer therapy protection
View Patent ↗A method of inhibiting damage to non-cancerous cells in a human subject during chemotherapeutic treatment or radiation treatment of cancer cells in the human subject includes administering to the human subject arsenic and/or one or more compounds of arsenic in a therapeutically effective amount prior to treatment with radiation or one or more chemotherapeutic agents.
1. A method of inhibiting damage to the small intestine in a human subject resulting from chemotherapeutic treatment of cancer cells in the human subject, comprising:
a) administering to the subject arsenic and/or one or more compounds of arsenic in an amount from about 1 μg/kg/day to about 30 μg/kg/day; and
b) administering to the subject a therapeutically effective amount of one or more chemotherapeutic agents that activate p53, from one to eight days after the administration of the arsenic and/or one or more compounds of arsenic,
wherein the arsenic and/or one or more compounds of arsenic supress p53 activity and inhibit damage to the small intestine in the human subject resulting from administration of the one or more chemotherapeutic agents to the human subject.
2. The method of claim 1 , wherein the arsenic and/or one or more compounds of arsenic is administered to the human subject three to eight days prior to administering the one or more chemotherapeutic agents to the human subject.
3. A method of inhibiting damage to bone marrow cells in a human subject resulting from chemotherapeutic treatment of cancer cells in the human subject, comprising:
a) administering to the subject arsenic and/or one or more compounds of arsenic in an amount from about 1 μg/kg/day to about 30 μg/kg/day; and
b) administering to the subject a therapeutically effective amount of one or more chemotherapeutic agents that activate p53, from one to eight days after the administration of the arsenic and/or one or more compounds of arsenic,
wherein the arsenic and/or one or more compounds of arsenic suppress p53 activity and inhibit damage to the bone marrow cells in the human subject resulting from administration of the one or more chemotherapeutic agents to the human subject.
4. The method of claim 3 , wherein the arsenic and/or one or more compounds of arsenic are administered to the human subject three to eight days prior to administering the one or more chemotherapeutic agents to the human subject.
5. A method of inhibiting damage to the small intestine in a human subject resulting from radiation treatment of cancer cells in the human subject, comprising:
a) administering to the subject arsenic and/or one or more compounds of arsenic in an amount from about 1 μg/kg/day to about 30 μg/kg/day; and
b) administering to the subject a therapeutically effective amount of radiation that activates p53, from one to eight days after the administration of the arsenic and/or one or more compounds of arsenic,
wherein the arsenic and/or one or more compounds of arsenic suppress p53 activity and inhibit damage to the small intestine in the human subject resulting from administration of the radiation to the human subject.
6. The method of claim 5 , wherein the arsenic and/or one or more compounds of arsenic is administered to the human subject three to eight days prior to administering the radiation to the human subject.
7. A method of inhibiting damage to bone marrow cells in a human subject resulting from radiation treatment of cancer cells in the human subject, comprising:
a) administering to the subject arsenic and/or one or more compounds of arsenic to the subject in an amount from about 1 μg/kg/day to about 30 μg/kg/day; and
b) administering to the subject a therapeutically effective amount of radiation that activates p53, from one to eight days after the administration of the administration of the arsenic and/or one or more compounds of arsenic,
wherein the arsenic and/or one or more compounds of arsenic suppress p53 activity and inhibit damage to the bone marrow cells in the human subject resulting from administration of the radiation to the human subject.
8. The method of claim 7 , wherein the arsenic and/or one or more compounds of arsenic are administered to the human subject three to eight days prior to administering the radiation to the human subject.