IP Library Granted Patent US 9,778,264
Granted Patent B2
US 9,778,264 · App. 14/454,107 · Granted Oct 3, 2017

Identification and enrichment of cell subpopulations

Inventors: Scott J. Dylla (Emerald Hills, CA); Marianne Santaguida (Redwood City, CA); Wade C. Anderson (Fairfield, CA); Bob Y. Liu (South San Francisco, CA); Samuel A. Williams (San Mateo, CA)
Assignee: ABBVIE STEMCENTRX LLC
G01N33/57492A61K39/0011C12N5/0693
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Quick Facts
Patent No.
US 9,778,264
App. No.
14/454,107
Granted
Oct 3, 2017
Kind
B2
Abstract

Markers useful for the identification, characterization and, optionally, the enrichment or isolation of tumorigenic cells or cell subpopulations are disclosed.

Claims (24)

1. A method of producing an animal model comprising implanting a subject animal with an enriched tumorigenic cell population comprising tumorigenic cells and an anti-CD46 antibody associated with a detectable agent, wherein the tumorigenic cells have a marker phenotype comprising CD46 hi , and wherein the detectable agent comprises a fluorescent tag.

2. The method of claim 1 , wherein the enriched tumorigenic cell population is derived from a solid tumor obtained from a subject suffering from a neoplastic disorder selected from the group consisting of adrenal cancer, bladder cancer, cervical cancer, endometrial cancer, kidney cancer, liver cancer, lung cancer, ovarian cancer, colorectal cancer, pancreatic cancer, prostate cancer, breast cancer, head & neck cancer, and skin cancer.

3. The method of claim 2 , wherein the subject animal is an immunodeficient mouse.

4. The method of claim 3 , wherein the immunodeficient mouse is selected from the group consisting of a nude mouse, a SCID mouse, a NOD/SCID mouse and a Beige/SCID mouse.

5. The method of claim 1 , wherein the enriched tumorigenic cell population further comprises an anti-CD324 antibody associated with a second detectable agent and wherein the tumorigenic cells have a marker phenotype comprising CD46 hi CD324 + .

6. The method of claim 5 , wherein the tumorigenic cells have a marker phenotype comprising CD46 hi CD324 + CD66c − .

7. The method of claim 1 , wherein the enriched tumorigenic cell population is derived from a tumor that has been passaged through a non-human mammal.

8. A method of producing an animal model comprising implanting a subject animal with an enriched tumorigenic cell population comprising tumorigenic cells having a marker phenotype comprising CD46 hi CD324 + , an anti-CD46 antibody associated with a first detectable agent, and an anti-CD324 antibody associated with a second detectable agent, wherein the detectable agent comprises a fluorescent tag.

9. The method of claim 8 , wherein the subject animal is an immunodeficient mouse.

10. The method of claim 9 , wherein the immunodeficient mouse is selected from the group consisting of a nude mouse, a SCID mouse, a NOD/SCID mouse and a Beige/SCID mouse.

11. The method of claim 8 , wherein the enriched tumorigenic cell population is derived from a solid tumor obtained from a subject suffering from a neoplastic disorder selected from the group consisting of adrenal cancer, bladder cancer, cervical cancer, endometrial cancer, kidney cancer, liver cancer, lung cancer, ovarian cancer, colorectal cancer, pancreatic cancer, prostate cancer, breast cancer, head & neck cancer, and skin cancer.

12. The method of claim 8 , wherein the enriched tumorigenic cell population is derived from a tumor that has been passaged through a non-human mammal.

13. The method of claim 8 , wherein the tumorigenic cells have a marker phenotype comprising CD46 hi CD324 + CD66c − .

14. A method of producing an immunodeficient mouse animal model comprising implanting an immunodeficient mouse with an enriched tumorigenic cell population comprising tumorigenic cells having a marker phenotype comprising CD46 hi and an anti-CD46 antibody associated with a detectable agent, wherein the detectable agent comprises a fluorescent tag.

15. The method of claim 14 , wherein the immunodeficient mouse is selected from the group consisting of a nude mouse, a SCID mouse, a NOD/SCID mouse and a Beige/SCID mouse.

16. The method of claim 14 , wherein the enriched tumorigenic cell population is derived from a solid tumor obtained from a subject suffering from a neoplastic disorder selected from the group consisting of adrenal cancer, bladder cancer, cervical cancer, endometrial cancer, kidney cancer, liver cancer, lung cancer, ovarian cancer, colorectal cancer, pancreatic cancer, prostate cancer, breast cancer, head & neck cancer, and skin cancer.

17. The method of claim 14 , wherein the enriched tumorigenic cell population is derived from a tumor that has been passaged through a non-human mammal.

18. The method of claim 14 , wherein the enriched tumorigenic cell population further comprises an anti-CD324 antibody associated with a second detectable agent and wherein the tumorigenic cells have a marker phenotype comprising CD46 hi CD324 + .

19. The method of claim 18 , wherein the tumorigenic cells have a marker phenotype comprising CD46 hi CD324 + CD66c − .

20. A method of producing an immunodeficient mouse animal model comprising implanting an immunodeficient mouse with an enriched tumorigenic cell population comprising tumorigenic cells having a marker phenotype comprising CD46 hi CD324 + , an anti-CD46 antibody associated with a first detectable agent, and an anti-CD324 antibody associated with a second detectable agent, wherein the detectable agent comprises a fluorescent tag.

21. The method of claim 20 , wherein the immunodeficient mouse is selected from the group consisting of a nude mouse, a SCID mouse, a NOD/SCID mouse and a Beige/SCID mouse.

22. The method of claim 20 , wherein the enriched tumorigenic cell population is derived from a solid tumor obtained from a subject suffering from a neoplastic disorder selected from the group consisting of adrenal cancer, bladder cancer, cervical cancer, endometrial cancer, kidney cancer, liver cancer, lung cancer, ovarian cancer, colorectal cancer, pancreatic cancer, prostate cancer, breast cancer, head & neck cancer, and skin cancer.

23. The method of claim 20 , wherein the enriched tumorigenic cell population is derived from a tumor that has been passaged through a non-human mammal.

24. The method of claim 20 , wherein the tumorigenic cells have a marker phenotype comprising CD46 hi CD324 + CD66c − .

Assignments (3)
MERGER Recorded Aug 7, 2016
From: STEMCENTRX, INC.
To: ABBVIE STEMCENTRX LLC
Reel/Frame 039601/0189 →
CHANGE OF NAME Recorded Apr 6, 2015
From: STEM CENTRX, INC.
To: STEMCENTRX, INC.
Reel/Frame 035375/0341 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 9, 2014
From: DYLLA, SCOTT J.; SANTAGUIDA, MARIANNE; ANDERSON, WADE C.; LIU, BOB Y.; WILLIAMS, SAMUEL A.
To: STEM CENTRX, INC.
Reel/Frame 033700/0098 →
Continuity (8)
Continuation PCTUS2013025361 · Feb 8, 2013
Continuation In Part 13820061
Continuation 13414666 · Mar 7, 2012
Continuation In Part 13369277 · Feb 8, 2012
Continuation PCTUS2011050451 · Sep 2, 2011
Provisional Application 61510413 · Jul 21, 2011
Provisional Application 61380181 · Sep 3, 2010
Related Publication 20150030636A1 · Jan 29, 2015