IP Library Granted Patent US 9,539,290
Granted Patent B2
US 9,539,290 · App. 14/140,345 · Granted Jan 10, 2017

Individualized bacterial treatment of pancreatic cancer

Inventors: Ming Zhao (San Diego, CA); Fuminari Uehara (San Diego, AZ)
Assignee: AntiCancer Inc.
A61K35/74C12N1/20C12N1/36
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Quick Facts
Patent No.
US 9,539,290
App. No.
14/140,345
Filed
Dec 24, 2013
Granted
Jan 10, 2017
Kind
B2
Art Unit
1645
USPC
435/7.32
Abstract

An individualized bacterial treatment of cancer is provided. The treatment includes a strain of bacteria modified by in-vivo passage through tumor grafts in experimental animals, where the modified strain exhibits enhanced cancer cell-targeting of a specific malignancy arising in a unique individual to the corresponding parent strain of bacteria. The treatment uses this modified strain for the treatment human solid-tumor malignancies by inoculating an individual with a quantity of the strain; and repeating inoculations at periodic intervals where repeated inoculations tend to progressively eliminate the solid tumor malignancy in the individual.

Claims (35)

1. A method for creating a strain of enhanced cancer cell-targeting bacteria for individualized cancer therapy, said method comprising:

(a) harvesting cancer cells from an individual;

(b) transplanting a quantity of said cancer cells into a quantity of experimental animals;

(c) incubating the experimental animals to establish a cancer tissue graft within the experimental animals;

(d) inoculating a Salmonella typhimurium A1 into a said experimental animal containing established said cancer tissue graft;

(e) removing said cancer tissue graft from said experimental animal inoculated with said Salmonella typhimurium A1 following a period of incubation of the inoculated said experimental animal;

(f) extracting a Salmonella typhimurium A1-R from said cancer tissue graft removed from the experimental animal inoculated with said Salmonella typhimurium A1-R ;

(g) incubating said Salmonella typhimurium A1-R under conditions suitable for bacterial multiplication;

(h) selecting a said Salmonella typhimurium A1-R ;

(i) incubating the selected said Salmonella typhimurium A1-R under conditions suitable for bacterial multiplication;

(j) inoculating a quantity of selected said Salmonella typhimurium A1-R into a second said experimental animal containing established said cancer tissue graft;

(k) removing said cancer tissue graft from the said experimental animal inoculated with a quantity Salmonella typhimurium A1-R following a period of incubation;

(l) extracting Salmonella typhimurium A1-R from said cancer tissue graft removed from the experimental animal;

(m) incubating said bacteria R1 under conditions suitable for bacterial multiplication; and

(n) selecting a Salmonella typhimurium R1 .

2. The method of claim 1 wherein said enhanced cancer cell-targeting bacteria is created by at least one passage through cancer cells in vitro.

3. The method of claim 1 wherein the Salmonella typhimurium A1 is auxotrophic for one or more essential nutrients.

4. The method of claim 1 wherein the Salmonella typhimurium A1 is auxotrophic for arginine and leucine.

5. The method of claim 1 further comprising creating additional strains of enhanced cancer cell-targeting Salmonella typhimurium A1 in response to repeating a portion of the method n additional times sequentially with strains of said Salmonella typhimurium A-Rn .

6. The method of claim 1 further comprising labeling the Salmonella typhimurium A1 with a fluorescent label.

7. The method of claim 1 further comprising labeling the Salmonella typhimurium A1 with a fluorophore.

8. The method of claim 1 further comprising labeling the Salmonella typhimurium A1 with a fluorescent protein.

9. The method of claim 1 further comprising labeling the Salmonella typhimurium A1 with a fluorescent antibody.

10. The method of claim 1 further comprising labeling the nuclei of the harvested cancer cells with a fluorescent label.

11. The method of claim 1 further comprising labeling the nuclei of the harvested cancer cells with a fluorescent protein; and a fluorescent antibody.

12. The method of claim 1 further comprising labeling cytoplasm of the harvested cancer cells with a fluorescent label.

13. The method of claim 1 further comprising labeling cytoplasm of the harvested cancer cells with a fluorophore.

14. The method of claim 1 further comprising labeling cytoplasm of the harvested cancer cells with a fluorescent protein.

15. The method of claim 1 further comprising labeling cytoplasm of the harvested cancer cells with a fluorescent antibody.

16. The method of claim 1 further comprising labeling the nucleus and the cytoplasm of the harvested cancer cells with fluorescent labels.

17. The method of claim 1 , wherein said cancer cells are a pancreatic cancer.

18. The method of claim 1 , wherein said cancer cells are a sarcoma.

19. The method of claim 1 , wherein said cancer cells are a lung cancer.

20. The method of claim 1 , wherein said cancer cells are a breast cancer.

21. The method of claim 1 , wherein said cancer cells are a colon cancer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 27, 2014
From: ZHAO, MING; UEHARA, FUMINARI
To: ANTICANCER INC.
Reel/Frame 032051/0897 →
Continuity (2)
Provisional Application 61745731 · Dec 24, 2012
Related Publication 20140178341A1 · Jun 26, 2014