IP Library Granted Patent US 11,840,732
Granted Patent B2
US 11,840,732 · App. 16/347,763 · Granted Dec 12, 2023

Diagnostic methods

Inventors: Göran Landberg (Gothenburg, SE); Anders Ståhlberg (Gothenburg, SE); Joakim Håkansson (Borås, SE)
Assignee: ISCAFF PHARMA AB
C12Q1/6886C12M25/14C12N5/0631G01N33/57415C12N2502/30C12N2533/90C12Q2600/106C12Q2600/136C12Q2600/158
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Quick Facts
Patent No.
US 11,840,732
App. No.
16/347,763
Granted
Dec 12, 2023
Kind
B2
Abstract

A method for determining one or more tumour properties in a subject with a tumour, the method comprising:—seeding a cell-free scaffold obtained from the tumour with cancer cells;—culturing the cancer cells in the scaffold;—assaying the cultured cancer cells for the presence of target molecules indicative of the expression of one or more genes in the cells; and—determining one or more tumour properties based on the results of the assay.

Claims (25)

1. A method for determining one or more properties of a tumour in a patient, the method comprising:

seeding a 3-dimensional cell-free scaffold obtained from the tumour in the patient with cancer cells, wherein the cancer cells are not taken from the tumour in the patient;

culturing the cancer cells in the scaffold;

assaying the cultured cancer cells for the presence of target molecules indicative of the expression of one or more genes in the cells; and

determining one or more properties of the tumour from which the 3-dimensional cell-free scaffold was obtained based on the presence of target molecules indicative of the expression of one or more genes in the cells in the assay; and wherein the one or more genes are selected from the group consisting of:

ACTN1; AIFM1; ALDH2; ALDOA; ANXA1; AP1B1; AP2B1; ATM; ATXN1; BAG2; BAG3; BHLHE40; BIRC5; BTBD2; BYSL; C3; CAMK2B; CAMK4; CARD11; CASP3; CAV1; CEACAM1; CHD3; COL17A1; CRCT1; DAPK1; DMD; DPYSL2; DYSF; E2F1; EGFR; EIF2AK3; EP300; EPOR; ERBB3; ESR1; FANCC; FEN1; FHIT; FKBP5; FN1; FOS; FRMD6; GADD45A; GADD45G; GOLM1; GSN; GSTP1; HCK; HDAC5; HSPB1; HSPD1; IGF1R; IL4R; ITGA6; ITGB4; JAK1; JUN; KAT2B; KIF15; KRT18; KRT8; LYST; LRP1; LRPS; MAP2; MAP3K14; MAP3K5; MAPK3; MAPKAPK3; MST1R; NDRG1; NME1-NME2; NOS3; NPAS2; NPHP1; NQO1; NR3C; PIK3CG; PAEP; PAK1; PARK2; PARP1; PDE4D; PFN2; PIM1; PTN; PKD1; PLA2G4A; PLD1; PPARGC1A; PPL; PPM1A; PPP1R15A; PPP2R1B; PRKCA; PRNP; PSG9; PSME3; RABAC1; RAC2; RASA1; RBL1; RGS2; RPS6KA3; RUNX1T1; SH2B3; SH3GL3; SLC9A3R1; SMAD4; SNX9; SORBS2; SOX9;SP1; SPG7; SREBF1; STUB1; SUMO4; SVIL; TGFB1 11; TH; TNFAIP3; TNFRSF14; TNIK; TP73; TPD52L1; TRIO; TUBA1A; VIM; WEE1; XPO5;YAP1; and ZNF259.

2. A method according to claim 1 wherein the tumour is a breast cancer tumour.

3. A method according to claim 1 wherein the one or more properties of the tumour from which the 3-dimensional cell-free scaffold was obtained are selected from invasiveness, migration, tumour malignancy grade, tumour malignancy potential, tumour recurrence, resistance to treatment and tumour proliferation.

4. A method according to claim 1 wherein the one or more genes are one or more markers of tumour progression.

5. A method according to claim 4 wherein the one or more markers of tumour progression are selected from markers of proliferation, markers of differentiation, markers of cancer stem cells, and markers of epithelial-mesenchymal transition (EMT).

6. A method according to claim 1 wherein the cancer cells are breast cancer cells.

7. A method according to claim 6 wherein the cancer cells are selected from MCF7, MDA231 and T47D cells.

8. A method according to claim 1 which further comprises obtaining the 3-dimensional cell-free scaffold from the tumour in the patient.

9. A method for determining a suitable treatment for a patient with a tumour, the method comprising:

determining one or more properties of the tumour from which the 3-dimensional cell-free scaffold was obtained by a method according to claim 1 ; and

determining a suitable treatment based on the properties of the tumour from which the 3-dimensional cell-free scaffold was obtained.

10. A method of treating a patient with a tumour, the method comprising:

determining the suitability of a treatment in the patient by a method according to claim 9 ; and

applying the treatment to the patient.

11. A method of treating patient with a tumour, the method comprising:

determining one or more properties of the tumour from which the 3-dimensional cell-free scaffold was obtained in the patient by a method according to claim 1 ;

selecting a suitable treatment based on the one or more properties of the tumour from which the 3-dimensional cell-free scaffold was obtained; and

providing the treatment to the patient.

12. A method according to claim 1 , wherein the patient is a human patient.

13. A method according to claim 2 wherein the one or more properties of the tumour from which the 3-dimensional cell-free scaffold was obtained are selected from invasiveness, migration, tumour malignancy grade, tumour malignancy potential, tumour recurrence, resistance to treatment and tumour proliferation.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 10, 2021
From: RISE RESEARCH INSTITUTES OF SWEDEN AB
To: ISCAFF PHARMA AB
Reel/Frame 058358/0021 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 10, 2021
From: HÅKANSSON, JOAKIM
To: ISCAFF PHARMA AB
Reel/Frame 058358/0044 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 15, 2020
From: LANDBERG, GORAN; STAHLBERG, ANDERS
To: ISCAFF PHARMA AB
Reel/Frame 054652/0620 →
Priority Claims (1)
GB 1618743 · Nov 7, 2016 · national
Continuity (1)
Related Publication 20190284638A1 · Sep 19, 2019