阅读说明：本技术 抗癌用组合物 (Anticancer composition ) 是由 金泰勋 朴全义 李庭旼 于 2019-09-19 设计创作，主要内容包括：公开一种包含曲贝德生及IL-2的抗癌用配合组合物。(Disclosed is a pharmaceutical composition for anticancer use, which comprises trabeculoside and IL-2.)

1. An anticancer compound composition containing trabeculoside and IL-2 is provided.

2. The anticancer complex composition of claim 1, wherein the trabeculodine and the IL-2 are administered simultaneously, sequentially or separately.

3. The anticancer complex composition of claim 1, which is used for treating solid cancer.

4. The anticancer complex composition of claim 3, wherein the solid cancer is breast cancer, pancreatic cancer, melanoma, lung cancer or rectal cancer.

5. An anticancer composition containing trabectedsen for combined administration with IL-2.

6. The anticancer composition for treating solid cancer according to claim 5.

7. The anticancer composition as set forth in claim 6, wherein the solid cancer is breast cancer, pancreatic cancer, melanoma, lung cancer or rectal cancer.

8. An anticancer composition containing IL-2 for combined administration with Tribexate.

9. The anticancer composition for treating solid cancer according to claim 8.

10. The anticancer composition as set forth in claim 9, wherein the solid cancer is breast cancer, pancreatic cancer, melanoma, lung cancer or rectal cancer.

Technical Field

The present invention relates to a complex composition for anticancer. More particularly, the present invention relates to a complex composition for anticancer comprising trabedersen and IL-2 and its co-administration.

Background

Since the conventional cytotoxic anticancer agents have a problem of attacking not only cancer cells but also normal cells, targeted therapeutic anticancer agents have become the mainstream of anticancer therapeutic agent development to improve the problem. Targeted therapeutic anticancer agents selectively attack only specific targeting factors in the carcinogenic process, and do not attack normal cells, and thus are considered to cause less pain to patients than the original cytotoxic anticancer agents.

However, such targeted therapeutic anticancer agents also have found a disadvantage of generating drug resistance after administration. In order to overcome the disadvantages of such targeted therapeutic anticancer agents and to prolong survival by anticancer therapy, anticancer immune agents are becoming the core of anticancer therapeutic agent development.

The present invention aims to provide an anticancer agent which reduces side effects and enhances anticancer effects at the time of treatment, and a combination administration thereof.

[ Prior art documents ]

[ non-patent document ]

Schlingensiepen KH et al,Cancer Sci.2011；102:1193-200

Disclosure of Invention

Technical problem to be solved

The present invention aims to enhance the anti-cancer effect by means of the combined administration of trabectedsen as TGF-beta 2 inhibitor and IL-2.

Means for solving the problems

In order to solve the above problems, the present invention provides an anticancer composition comprising a TGF-beta inhibitor and a cytokine.

Specifically, the present invention provides an anticancer complex composition comprising trabedersen (trabedersen) as a TGF- β inhibitor and Interleukin (IL) -2.

Expression of TGF- β in tumors performs a global immunosuppressive function. TGF- β is a biomarker that exhibits resistance to an anticancer immune agent drug.

Since immune checkpoints (immune checkpoint) such as PD-1 and PD-L1 play a part of the role in global immunosuppression, attempts to restore immune functions only partially, and fail to completely restore apoptotic functions of the immune system, have been made by using inhibitors against immune checkpoints such as PD-1 and PD-L1 as an anticancer immune agent without removing TGF- β.

Trabedersen (Trabedersen) was a synthetic 18-mer phosphorothioate antisense oligonucleotide specifically developed targeting human TGF- β, developed based on data showing a correlation of TGF- β overexpression with tumor progression. The correlation of TGF-. beta.overexpression with tumor progression has been evaluated in a number of in vitro (in-vitro) and in vivo (in-vivo) non-clinical models (Schlinggenepen KH et al, Cancer Sci.2011; 102: 1193-.

IL-2 (interleukin-2), one of cytokines (cytokines), stimulates the immune system, widely increasing the size of immune cells.

ADVANTAGEOUS EFFECTS OF INVENTION

The anticancer agent combination composition of the invention can reduce side effects during administration and simultaneously synergistically enhance the anticancer effect.

Drawings

FIG. 1 shows the results of the relative qualitative analysis of TGF-. beta.1 mRNA and TGF-. beta.2 mRNA from various cancer cell lines.

FIG. 2 is a graph showing the results of quantitative analysis of TGF-. beta.1 mRNA of various cancer cell lines.

FIG. 3 is a graph showing the results of quantitative analysis of TGF-. beta.2 mRNA of various cancer cell lines.

Fig. 4 to 8 illustrate the results of the growth inhibition assay in breast, pancreatic, melanoma, lung, and rectal cancer (colorectal cancer) cell lines using trabectedsen alone treatment of EZCYTOX, respectively.

Figures 9 to 13 illustrate the effect of apoptosis in human PBMC activated with L-2 used in combination with trabeculogen.

FIGS. 14 and 15 are graphs showing the in vivo anti-cancer effect of IL-2 in combination with Tribexate in human PBMC-activated (humanized) immunodeficient mice (NSG mouse).

Detailed Description

The present invention relates to an anticancer complex composition comprising trabeculogen and IL-2. The compositions of the invention are particularly useful for the treatment of solid cancers (e.g., breast, pancreatic, melanoma, lung or rectal cancer, etc.).

In the administration of the composition of the present invention, trabectedin and IL-2 may be administered in combination by sequential or simultaneous administration or by separate administration. Thus, the compositions of the present invention, when administered, exhibit synergistic effects with each other in vivo, in which the components are present together in therapeutically effective amounts.

In another aspect, the present invention relates to an anti-cancer composition comprising trabectedsen for administration in combination with IL-2. Such compositions of the invention are particularly useful for the treatment of solid cancers (e.g., breast, pancreatic, melanoma, lung or rectal cancer, etc.).

In yet another aspect, the present invention relates to an anti-cancer composition comprising IL-2 for administration in combination with trabectedson. The compositions of the invention are particularly useful for the treatment of solid cancers (e.g., breast, pancreatic, melanoma, lung or rectal cancer, etc.).

The present invention will be described in detail below with reference to examples. However, the following examples are only illustrative of the present invention, and the spirit and scope of the present invention is not limited thereto.

In order to confirm the anticancer effect of the composition of the present invention, an in vitro (in-vitro) anticancer effect experiment using trabectedsen as a TGF- β 2 inhibitor in combination with IL-2 was performed in a mouse solid cancer model. For example, the expression level of TGF-. beta.mRNA was confirmed in various solid cancer cell lines, and among them, the apoptosis effect of cancer cells was confirmed by treating Trabecten alone or in combination with PBMC (peripheral blood mononuclear cell) that activates immune cells (activation) with IL-2. In addition, in the addition of human PBMC to humanized immunodeficiency mice, confirmed the Traberson and IL-2 combined use of human cancer cells (xenograft model) growth inhibition effect.

Experimental example 1: quantitative and relatively qualitative analysis of TGF-beta 2mRNA level for multiple cancers

1) TGF-beta 2mRNA expression analysis

Experiments were performed using the cell lines shown in table 1 below.

[ Table 1]

From each cell line 1X10 of Table 1 above, an RNA prep kit (Qiagen, Germany) was used⁷RNA was extracted (preparation) from each, and then cDNA was synthesized at 37 ℃ for 1 hour using 1. mu.g of the extracted RNA as a template.

PCR was performed on 10. mu.l of cDNA (denaturation 95 ℃ for 1 min, annealing 57 ℃ for 1 min, extension 72 ℃ for 1 min, cycles 35 and final extension 72 ℃ for 5 min) using TGF-. beta.2 specific primers (specific primers) F (ATCGATGCACCTCCAACATTG) and R (GCGAAGGCAGCAATTATGCTG). Then, the results of PCR with GAPDH (Glyceraldehyde-3-phosphate dehydrogenase) confirmed the mRNA expression of TGF-. beta.1 and TGF-. beta.2 by the band intensities of TGF-. beta.1 and TGF-. beta.2.

FIGS. 1 to 3 show the results of relative qualitative and quantitative analysis of TGF-. beta.1 or TGF-. beta.2 mRNA.

As a result of the experiment, it was found that TGF-. beta.mRNA was expressed relatively much in skin cancer cells, lung cancer cells and breast cancer cells.

Experimental example 2: apoptosis effects of trabectedsen alone in multiple solid cancer cell lines

The apoptosis effect of trabeculowny alone was confirmed in multiple solid cancer cell lines.

1) Cell culture

As shown in Table 1 above, according to the cell type, a medium such as RPMI1640 (10% FBS, antibacterial-antifungal agent, HEPES), DMEM (10% FBS, antibacterial-antifungal agent) or the like was used, and the cells were cultured at 37 ℃ and CO₂Culturing under 5% environment.

2) Transfection of Tribexad (transfection)

Each of the cell lines shown in Table 1 was inoculated (seeded) at 37C and 5% CO as shown in Table 2 below₂After 24 hours of incubation under conditions, the transfection was carried out with Tribexagen.

The specific transfection method is as follows:

tribexate was diluted in Serum-free medium (culture solution A: RPMI1640 or DMEM) so as to reach concentrations of 20nM, 40nM, 80nM and 160nM, respectively, in the finally prepared culture solution (i.e., the culture solution containing culture solution A, culture solution B and cell culture solution described below).

Liposome (Lipofectamine)2000 was quantitatively added to a serum-free medium (medium B: RPMI1640 or DMEM) so as to obtain the experimental conditions shown in Table 2 below.

After allowing the culture solution A and the culture solution B to react for 5 minutes at room temperature, 50ul of the culture solution A and 50ul of the culture solution B (1:1 by volume) were mixed on a 12-well plate basis, and then allowed to react for 20 minutes at room temperature.

After replacing the culture solution of the cells prepared in the "1) cell culture" step with a new 10% FBS culture solution, a mixture of the culture solutions a and B, which have completed the reaction, was added to the cell culture solution.

[ Table 2]

3) Cytotoxicity Assay (cytotoxin Assay)

For cytotoxicity analysis, the activity of the cells was measured at O.D 450nm by EZCYTOX (DAEILLAB service Co.) the next day after transfection with Trabecten, and Apoptosis (Apoptosis)/Necrosis (Neociss) analysis was performed by staining with Annexin V and PI and by using FACS (Fluorescence activated cell sorter).

FIGS. 4 to 8 are the results of analysis of growth inhibition by the EZCYTOX of Tribexate alone in cancer cell lines. It is known that the activity of cancer cell lines is inhibited by the administration of trabeculowny. However, in the Capan-2 and SK-MEL-28 cell lines, less apoptosis was observed.

Experimental example 3: apoptosis test in breast cancer cell lines using IL-2-activated human PBMC in combination with trabeculogen

1) IL-2 activation

PBMC (peripheral blood mononuclear cell: peripheral b) of peripheral blood was isolated using ficoll-plane plus (purchased from general electric medical group)LOOD MONONUCLEAR CELL), 4X10 in culture medium supplemented with 10% FBS, IL-2(20ng/ml)⁶Culture at a concentration of/ml, and the expression of CD69(T cell activation marker) was confirmed in CD4+/CD8+ T cells on the fifth day by FACS.

2) IL-2 and trabeculogen combination dosing assay

PBMC of peripheral blood were isolated by ficoll-plane plus (general electric medical treatment group) as described above, and then cultured in a culture medium containing 10% FBS and IL-2(20ng/ml) at 4X10⁶Culture at a concentration of ml. On the third day of culture, after transfection (transfection) of the cancer cells with trabeculogen, 24 hours later, the culture medium of the target cancer cells was changed to 10% FBS culture medium, and on the fifth day of IL-2 culture, PBMCs were expressed as cancer cell lines (seeding): effector (immune effector cell) ═ 1: 10 ratios (cell number ratio) were placed in 2ml of 10% FBS RPMI medium, and then added to a well plate for culture.

Non-activated PBMCs were isolated separately using polysucrose and used as controls. In addition, cell lines without any PBMC added were also used as control groups. Experiments were performed with varying concentrations of trabecteds in the medium at transfection (i.e., for 0nM, 10nM, 40nM concentrations, respectively).

After 24 hours, the cytotoxicity (cytotoxicity) results were analyzed by PI staining.

Experimental example 4: apoptosis effect test using IL-2-activated human PBMC in combination with trabeculogen in pancreatic cancer cell lines

Experiments were carried out on a pancreatic cancer cell line (AspC-1) in a manner similar to that in Experimental example 3.

Experimental example 5: apoptosis effect experiment of IL-2activated human PBMC and Tribexagon combined in melanoma cell strain

Experiments were carried out on melanoma cell lines (Hs 294T) in a manner similar to that in experimental example 3.

Experimental example 6: apoptosis effect experiment using IL-2activated human PBMC and Tribeheny in lung cancer cell line

In a similar manner to Experimental example 3, an experiment was conducted on a lung cancer cell line (A549).

Experimental example 7: apoptosis effect experiment of human PBMC activated by IL-2 and trabeculogen combined in rectal cancer cell strain

Experiments were carried out on rectal cancer cell lines (HT29, DLD-1, LS174T) in a manner similar to that of Experimental example 3.

Fig. 9 to 13 illustrate the results of experiments in experimental examples 3 to 7. As shown in the figure, it was found that the apoptosis effect of trabecteds administered alone (non-activated PBMC, DMEM, or RPMI) or IL-2 administered alone (IL-2activated PBMC, 0nM) was greatly increased in the combination of trabecteds and IL-2 (IL-2activated PBMC).

Experimental example 8: (in vivo test) test of cancer growth inhibitory Effect of IL-2 in combination with Tribexagen in immunodeficient mice (NSG mouse) humanized with human PBMC in triple negative Breast cancer cell lines

In a mouse humanized by injecting human PBMC into an NSG (NOD/SCID/Gamma) immunodeficient mouse, experiments were carried out to confirm the effect on the growth of human Triple Negative Breast Cancer (TNBC) cell line MDA-MB-231 when trabeculogen alone was administered, when IL-2 alone was administered, and when trabeculogen and IL-2 were administered in combination, respectively

Experimental methods

Lyophilized powdery Tribexade (TBD) and liquid form recombinant human IL-2(rhIL-2, Korea JW CreaGene; Cat.No. JW-H031-0025) were prepared. The preservation conditions of the Tribexade are 2-8 ℃ and the preservation conditions of the gene recombinant human IL-2 are-80 ℃.

The trabeculogen is dissolved in sterilized normal saline for use. Gene recombination human IL-2 will be at a concentration of 25. mu.g/250. mu.l (2X 10)⁸IU/mg) solution was diluted just before administration.

NSG mice were divided into 10 groups of 6 mice each, and administered Intraperitoneally (IP) at the amounts shown in table 3 below.

[ Table 3]

Xenograft model fabrication

MDA-MB-231 cells were allowed to grow at 37 ℃ with 5% CO₂And (5) proliferating in a culture environment. RPMI1640 medium (including L-glutamine, 25mM HEPES) containing 10% FBS was used, and when the cells occupied 70-80% of the surface of the 25T flask, the seed culture was performed at a ratio of 1: 5.

On the day of tumor transplantation, the cultured tumor cells were arranged at 1X10⁷Cells/100. mu.l were suspended in PBS at 1X10⁷Cells/mouse, 100. mu.l were subcutaneously implanted in the right flank (flank) site of the mouse.

human-PBMC (Hu-PBMC) NSG mouse model fabrication

Human PBMC were thawed (bathing) in a 37 ℃ water bath (water bath), washed 2 times (bathing) with RPMI1640 containing 20% FBS (containing DNAse I), at 37 ℃ with 5% CO₂The culture environment is stable for 30 minutes.

After 30 min incubation, PBMC were diluted 5X 10 in PBS⁷To 10X 10⁷After cell/ml concentration, 1 mouse was treated at 1X10⁷Cell/dose was administered (PBMC administration third day after cancer cell administration).

Method of administration

In the mice to which PBMC was administered as described above, on the second day after PBMC administration (fifth day after cancer cell transplantation), trabectedsen was administered intraperitoneally at 1/2 day intervals for 8 times at the amounts shown in table 3, and on the fourth day after PBMC administration (seventh day after cancer cell transplantation), IL-2 was administered at 1/1 day intervals for 4 days at the amounts shown in table 3, and then the administration was stopped for 3 days, and this was used as one cycle, and two cycles were administered intraperitoneally.

The schedule of inoculation, PBMC administration, trabectedsen administration and IL-2 administration was as follows:

tumor Volume (Tumor Volume) measurement

Tumor volumes were measured 1/2 days from the time of dosing with trabeculodine and/or IL-2. That is, tumor volume was measured at 1/2 days from day 5 after tumor inoculation (day 0). Tumor volume the size of the cancer cell mass produced in the injected part was measured with a Caliper (Caliper: CD-15CPX, digital Caliper, Sanfeng, Japan) and the volume was calculated according to the following mathematical formula:

[ mathematical formula ]

Tumor volume (TV: mm)³)＝(W²×L)/2

In the above formula, W is the minor axis length and L is the major axis length.

The results of the above experiments revealed that the combined administration of trabecteden and IL-2 synergistically exhibited the growth inhibitory effect on cancer cells, as compared with the administration of either trabecteden alone or IL-2 alone (see fig. 14 and 15).

Industrial applicability

The anticancer compound composition can be used for anticancer administration.