IP Library Granted Patent US 8,795,738
Granted Patent B2
US 8,795,738 · App. 12/945,430 · Granted Aug 5, 2014

Use of arsenic for cancer therapy protection

Inventor: Zhi-Min Yuan (San Antonio, TX)
Assignee: Board of Regents of the University of Texas System
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Quick Facts
Patent No.
US 8,795,738
App. No.
12/945,430
Granted
Aug 5, 2014
Kind
B2
Abstract

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.

Claims (20)

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.

Assignments (3)
CONFIRMATORY LICENSE Recorded Mar 13, 2017
From: UNIVERSITY OF TEXAS HLTH SCIENCE CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 041980/0058 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2016
From: HA, CHUL SOO
To: BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 038294/0772 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 29, 2011
From: YUAN, ZHI-MIN
To: BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 026521/0566 →
Continuity (2)
Provisional Application 61260662 · Nov 12, 2009
Related Publication 20110250291A1 · Oct 13, 2011