Functional inhibition of F11 receptor (F11R/junctional adhesion molecule-A/JAM-A) activity by a F11R-derived peptide in breast cancer and its microenvironment

Purpose To examine the involvement of the F11R/JAM-A protein in breast cancer metastasis, we utilized the F11R/JAM-A antagonistic peptide 4D (P4D) in experiments of transendothelial migration (TEM) of breast cancer cells. Methods Experiments were conducted in the mouse 4T1 breast cancer model utilizing the human mammary epithelial cell and endothelial cell lines. The levels of soluble F11R/JAM-A (sJAM-A) in the murine plasmas were measured by ELISA. Levels of F11R/JAM-A mRNA and protein in cell lines were assessed by qRT-PCR and Western blot, respectively. Cell surface expression of F11R/JAM-A was demonstrated by flow cytometry. Functional tests included the TEM of breast cancer cells and adhesion of breast cancer cells to the endothelium. The endothelial permeability was studied by fluorescent tracer assay and by the Real-Time Cell Analysis (RTCA). Results The tumor inducers Tβ4 and TGF-β1 reduced the levels of sJAM-A in murine plasma, and reduced the F11R/JAM-A protein levels in the human microvascular endothelial cell line HMEC-1. The adhesion and TEM measured between breast cancer cells and inflamed or Tβ4-treated endothelium were inhibited by P4D. The presence of P4D did not destabilize the pre-existing tight junctions in the endothelial monolayer. The barrier-protecting effect of P4D was stronger than that of forskolin, when a booster dose of P4D was applied to the inflamed endothelium. Conclusions F11R/JAM-A protein can be considered as a novel target in the treatment of breast cancer metastasis. In vivo and clinical studies are needed to further investigate the effectiveness of F11R/JAM-A-derived peptide as a possible anti-metastatic drug. Electronic supplementary material The online version of this article (10.1007/s10549-019-05471-x) contains supplementary material, which is available to authorized users.


Background
Breast cancer is the leading cause of cancer death among females worldwide, [1] including Poland [2]. The majority of breast cancer-related deaths is caused by metastasis that is considerably promoted by inflammation [3]. The formation of metastasis is initiated by the adhesion of tumor cells to the endothelium and the subsequent transendothelial migration (TEM) of cancer cells [4]. This mechanism is not completely understood. Hence, we focused on the molecule involved in the adhesion of platelets to cytokine-inflamed endothelium, the F11 receptor (F11R, Junctional Adhesion Molecule-A, F11R/JAM-A, CD321), to examine its role in the early stages of metastasis. F11R/JAM-A is the tight junction (TJ) protein important for platelet and leukocyte interactions with the epithelium and endothelium [5][6][7][8][9][10][11][12]. Upon inflammation, F11R/ JAM-A is internalized from endothelial TJs into recycling endosomes and relocated to the apical endothelial surface that faces the vessel lumen [13]. F11R/JAM-A molecules are thereby able to interact with leukocyte surface proteins, including F11R/JAM-A (by trans-homodimerization) and integrins, thus promoting leukocyte TEM [6,[14][15][16][17]. Cancer cells cross the endothelial barrier in a similar manner to that of leukocytes [4].
The aberrant expression of F11R/JAM-A contributes to tumor progression [18] and its role is best studied in breast cancer [19][20][21][22][23][24][25]. However, the significance of F11R/JAM-A in breast cancer is controversial, since loss of F11R/JAM-A induces the breast cancer cell invasion [19][20][21], whereas the overexpression of this protein correlates with poor prognosis [22][23][24][25]. F11R/JAM-A was shown to promote TEM of monocytes in breast cancer [6] and to inhibit TEM of melanoma cells [15], but its direct effect on TEM of breast cancer cells has never been studied.
In order to define the role of F11R/JAM-A in breast cancer metastasis, we utilized a peptide derived from the sequence of the F11R/JAM-A protein, peptide 4D (P4D), which blocks the homophilic interactions between the F11R/ JAM-A molecules. We investigated how P4D influences the interactions between the breast cancer cells and endothelial cells in the mouse breast cancer model, and examined its effects on human cell lines treated with thymosin β4 (Tβ4), an inducer of metastasis [26], and linked with breast cancer [27][28][29]. Further cell treatment involved the use of the inflammatory cytokines. Both the formation of TJs and the interactions of cancer cells with the endothelium were blocked by P4D. We propose that P4D can be considered as the drug candidate for use in the prevention of breast cancer metastasis.

Mice mammary gland tumor culture and tumor induction
Female BALB/c mice aged 8-12 weeks from the Animal House of the Institute of Biology, University of Bialystok (Bialystok, Poland) were housed under standard conditions at the Animal House of the Medical University of Lodz (Lodz, Poland). The procedures were conducted as per the National Animal Care Committee regulations, and were approved by the Local Ethical Committee for Animal Research in Lodz (license number 9/LB51/2017). All efforts were made to minimize animal suffering.
Murine 4T1 cells (American Type Culture Collection, ATCC) were cultured in RPMI-1640 with 10% fetal bovine serum (FBS) in flasks to 80% confluence. The 4T1 cells were harvested, resuspended at a concentration of 10 4 cells in 100 µl PBS per mouse, and administered subcutaneously in inguinal nipple area. Seven days after the injections, the mice were divided into three groups: the Tβ4 group, the TGF-β1 group, and the control group (PBS). Non-control groups were given intraperitoneally Tβ4 or TGF-β1 resuspended in PBS at a concentration of 15 mg/1 kg body weight or 5 mg/1 kg body weight, respectively. Each injection was followed by 3 days of an injection-free period. After 21 days of treatment, the mice were anesthetized intraperitoneally with the ketamine and xylazine solution (0.1 ml/20 g mouse). Ten mice were used for each experimental group. Blood samples were collected by cardiac blood drawn using a syringe with K2-EDTA solution. Samples were centrifuged (662×g, 10 min, 4 °C), and the plasma was aliquoted and stored at − 80 °C for further analysis.

Cell treatment
The cells were cultured overnight in a serum-free medium and subsequently incubated for 0, 2, 5, 12, or 24 h with Tβ4 (100 nM), and then for 24 h with TGF-β1 (10 ng/ml), tumor necrosis factor-α (TNF-α; 10 ng/ml), or with a mixture of proinflammatory cytokines (TNF/IFN)-TNF-α (10 ng/ml) and interferon-γ (IFN-γ; 20 ng/ml). For the inhibition of TJ formation between the cancer cells and endothelium, the cells were treated with the P4D peptide with the sequence of a 70-82 amino acids fragment of the F11R/JAM-A mature polypeptide chain that is responsible for F11R/JAM-A transhomodimerization [31]. The peptide P4D is a d-amino acid analog of the native peptide that binds to the 70-82 amino acid fragments and blocks the trans-homodimerization of F11R/JAM-A molecules, thus inhibiting the TJs formation in the endothelial monolayer as well as between the cancer cells and endothelial cells [32]. The sequence of control peptide (Scr) corresponded to P4D peptide, but was scrambled by random insertion of amino acid residues during the synthesis process. The peptides were synthesized and purified by LifeTein, LLC and their sequences were as follows: NH 2 -(dK)-SVT-(dR)-EDTGT YTC -CONH 2 for P4D and NH 2 -S-(dK)-TVE-(dR)-TDTGTYC-OH for Scr. The cells were treated with P4D or Scr (500 µM) for 0, 1, 5, or 24 h. The cells incubated with forskolin (FSK; BioShop) for 24 h at a concentration of 10 µM served as the positive control of the junctions tightening for impedance-based measurements of endothelial permeability.

Enzyme-linked immunosorbent assay
F11R/JAM-A levels in murine plasma were assayed by RayBio ® Mouse JAMA ELISA Kit (RayBiotech) according to the manufacturer's protocol and measured spectrophotometrically using the Wallac 1420 VICTOR2 Multilabel Counter (PerkinElmer).

RT-PCR
Total RNA was isolated from the cells with the TriPure Reagent (Roche) due to the manufacturer's protocol, dissolved in nuclease-free water, and analyzed spectrophotometrically for concentration and purity. The RNA concentrations in all samples were equalized and RNA was transcribed to cDNA using the iScript cDNA Synthesis Kit (BioRad) according to the manufacturer's instructions. The cDNA samples were amplified by the Dream Taq Green PCR Master Mix (Thermo) and the Whatman Biometra T3 Thermocycler (Biometra) according to the provided instructions. The specific oligonucleotide primer pairs were synthesized (Genomed, Warsaw, Poland) and used in PCR reactions for the following transcripts: forward 5′-CGA GAG GAA ACT GTT GTG CC-3′ and reverse 5′-AAC GAG TCT GGT GGT GTC TC-3′ for F11R/JAM-A, forward 5′-GAG AGA TGA TGA CCC TTT TGGC-3′ and reverse 5′-CCA TCA CCA TCT TCC CAG GAGCG-3′ for glyceraldehyde 3-phosphate dehydrogenase (GAPDH, used as the loading control). The amplified products were separated in 7% polyacrylamide gels in Tris-acetate-EDTA buffer (TAE; tris(hydroxymethyl) aminomethane; ethylenediaminetetraacetic acid). Bands were visualized by ethidium bromide and UV light and documented using Gel Doc 2000 (BioRad).

Western blot
The cells were lysed with lysis buffer (1% Triton X-100, 0.1% SDS, and protease inhibitors in PBS). The protein concentrations were determined with the BCA Protein Assay Kit (Thermo). Cell lysates (50 µg proteins per sample) were boiled in the loading buffer (50 mM Tris-HCl, pH 6.8, 8% glycerol, 2% SDS, 5% β-mercaptoethanol, 0.002% bromophenol blue), separated under reducing conditions on 4-20% gradient SDS-PAGE gels (BioRad), and electroblotted (120 min, 200 mA, 4 °C) onto polyvinylidene difluoride (PVDF) membranes (BioRad). The membranes were blocked for 2 h at room temperature with Tris-buffered saline (TBS) containing 5% non-fat dry milk and incubated overnight at 4 °C with a primary antibody diluted in TBS containing 0.05% Tween 20 (TBST). The following primary antibodies were used: monoclonal rabbit anti-JAM-A (Abcam) and monoclonal mouse anti-GAPDH (R&D Systems). The membranes were washed with TBST and incubated for 1 h at room temperature with the corresponding HRP-conjugated secondary antibodies (Santa Cruz) and processed for chemiluminescent detection using Westar ηC ECL Substrate (Cyanagen). The images were documented by ChemiDoc MP Imager (BioRad) and analyzed densitometrically with ImageJ software (National Institute of Health, USA). GAPDH bands served as loading controls.

Flow cytometry
The cells were labeled with the FITC anti-human CD321 (F11R/JAM-A) Mouse IgG 1 Antibody or with the relevant isotype control (BioLegend). Labeled cells were washed, harvested with ice cold EDTA/PBS, fixed with BD CellFix (Becton-Dickinson), and analyzed by FACS Canto II flow cytometer (Becton-Dickinson) upon the fluorescence excitation at 488 nm and the emission at 517 nm. Data were recorded with DIVA (Becton-Dickinson) and analyzed using FCSalyzer software (https ://sourc eforg e.net/proje cts/fcsal yzer/).

Adhesion of breast cancer cells to endothelial monolayer
Two days after seeding, HMEC-1 cells have formed the confluent monolayers in the wells of 24-well plates and were subjected to a suitable treatment. Mammary epithelial cells (MECs) were starved overnight and on the assay day were labeled with CellTracker Green CMFDA Dye (Molecular Probes). Just before the assay, the HMEC-1 cells culture medium was substituted with the adhesion medium (MCDB 131 containing 1 mM CaCl 2 , 1 mM MgCl 2 , and 1% bovine serum albumin). Subsequently the aliquots of MECs (1 × 10 5 /well) were applied onto the endothelial monolayers and allowed to adhere for 1 h in a humidified incubator (37 °C, 5% CO 2 ). Non-adherent cells were washed away by PBS. The adherent cells were lysed by 2% SDS, and the fluorescence was measured using the Wallac 1420 VICTOR2 Multilabel Counter at 492 nm of excitation and 517 nm of emission wavelengths.

Transmigration of MECs across the endothelium
HMEC-1 cells were cultured in Transwell units with polycarbonate filter and 8 μm pores (Costar) in 24-well plates for 2 days at 37 °C to confluence. MECs were starved overnight and labeled with CellTracker Green CMFDA Dye. An aliquot (1 × 10 5 /well) of fluorescent MECs in serum-free medium was added in the top of the Transwell chamber, whereas the conditioned medium was used as a chemoattractant in the lower compartment. The wells containing the serum-free medium in the lower compartment were used to estimate the background migration. MECs were migrating across the endothelial monolayer for 6 h in a humidified incubator (temperature of 37 °C and 5% CO 2 atmosphere). At the end of the assay, non-migrated cells were wiped out from the inner surface of the membrane with a cotton swab. The assay was documented at 200 × magnification with a fluorescent inverted microscope and a digital camera (Zeiss). The migrated cells (five randomly chosen fields of each well) were counted using the ImageJ software.

Macromolecular permeability of endothelial monolayer
Endothelial permeability was analyzed by macromolecular tracer assay. HMEC-1 cells were grown in Transwell inserts with polyethylene terephthalate filters and 0.4-μm pores in 24-well plates at 1.5 × 10 5 cells/insert and immediately treated with P4D or Scr peptide at a concentration of 500 μM (the samples indicated as 0 h of incubation). Non-treated cells served as a control sample (Ctrl). Moreover, HMEC-1 cells were treated with the peptides at 1, 5, or 24 h after seeding. One hour after the last treatment FITC-dextran with a molecular weight of 40 kDa was added into the inserts and the culture medium from the wells was replaced with PBS. After 1 h of incubation in darkness in a humidified incubator (37 °C, 5% CO 2 ), the PBS from the wells (outside the inserts) was transferred into the wells of a black 96-well plate and the fluorescence was measured using the Wallac 1420 VICTOR2 Multilabel Counter at 492 nm of excitation and 517 nm of emission wavelengths.

Impedance-based measurement of endothelial permeability
Experiments based on impedance measurements were performed at Bionanopark, Ltd. (Lodz, Poland) with the ACEA xCELLigence ® Real-Time Cell Analysis (RTCA) DP system (Roche) according to the manufacturer's instructions. Briefly, HMEC-1 cells were seeded at 40,000 cells per well and the plates were locked into the RTCA instrument for continuous recording of impedance changes expressed as Cell Index (CI) values [33]. During the phase of logarithmic cell growth HMEC-1 cells were pretreated with cytokines (TNF/IFN) and 24 h later they were treated with the tested compounds (Scr, P4D, or FSK). Alternatively, the cells were treated with the compounds 2 h after the cytokine treatment or the compound treatment was applied about 3 h after HMEC-1 seeding and about 67 h later was followed by the cytokine treatment. For the sample designated as 'P4D & TNF/IFN' after the pretreatment with P4D, the cells were subjected to the concurrent treatment with P4D and cytokines.

Statistical analysis
The results are presented as arithmetic mean ± standard deviation (SD) of at least three independent experiments. The data were analyzed by one-way ANOVA with the Tukey's post hoc multiple comparisons test using the GraphPad Prism software (GraphPad Software). Differences were considered statistically relevant at P < 0.05.

Tβ4 and TGF-β reduce the plasma level of soluble F11R/JAM-A
Experiments were performed in vivo in the murine 4T1 breast cancer model [34][35][36]. Plasma samples obtained from the blood of 4T1-treated mice and untreated mice were analyzed by ELISA for soluble F11R/JAM-A (sJAM-A) quantitation. The injection of 4T1 cells did not change the level of sJAM-A in the murine plasma (Fig. 1). However, a significant decrease in the murine plasma level of sJAM-A was found upon the administration of either Tβ4 or TGF-β1 ( Fig. 1 and Supplementary Table S1).
The expression of F11R/JAM-A was examined on nontumorigenic human breast epithelial cells and on tumorigenic cells by flow cytometry (Fig. 2a). The lowest level of F11R/JAM-A/CD321 was detected on the surface of tumorigenic MDA-MB-231 cells (green). The tumorigenic MCF-7 cells and the non-tumorigenic MCF-10A cells exhibited similar F11R/JAM-A protein levels (Fig. 2a).
The administration of Tβ4 or TGF-β1 significantly dropped the F11R/JAM-A levels in the murine plasma (Fig. 1). Consequently, we examined whether these molecules could affect the expression of F11R/JAM-A on the protein and/or message level. The presence of either Tβ4 or TGF-β1 did not alter F11R/JAM-A message in treated cells (Fig. 2b, d). However, Tβ4 significantly decreased the level of the F11R/JAM-A protein in HMEC-1 cells after a 24-hour incubation period similar to TGF-β1 that was used as the positive control for demonstrating the F11R/JAM-A downregulation (Fig. 2c) [20]. The incubation of cells with Tβ4 for up to a 12-hr period of time resulted in significant time-dependent changes in the F11R/JAM-A protein level (Fig. 2e).

F11R/JAM-A derived peptide 4D (P4D) blocks TEM of breast cancer cells
The soluble form of F11R/JAM-A was reported to inhibit both the human platelet aggregation induced by a stimulatory monoclonal antibody M.Ab.F11 and the platelet adhesion to the inflamed endothelium [5,7,10,31]. The F11R/ JAM-A antagonistic peptide 4D (P4D) also blocked the M.Ab.F11-induced aggregation and the adhesion of platelets to activated endothelial cells. Consequently, we speculated whether the decrease in the plasma level of sJAM-A produced by Tβ4/TGF-β1 could interfere with adhesive processes and thereby promote the transendothelial migration (TEM) of breast cancer cells. Thus, we examined the interactions between mammary epithelial cells (MECs) and endothelial cells in the presence of the P4D peptide (Fig. 4).
The cytokines TNF-α and IFN-γ (TNF/IFN) enhanced the adhesion of MECs to the endothelium (Fig. 4a). The addition of P4D significantly inhibited the adhesion of MECs to the inflamed endothelium and this effect was the most pronounced for MDA-MB-231 cells (Fig. 4a). Likewise, we observed that the TEM of breast cancer cells in the presence of TNF/IFN and Tβ4 was blocked by P4D ( Fig. 4b and Supplementary Fig. S1). Tβ4 activates the cellular motility and inhibits the adhesion [37], thus we did not utilize this peptide for adhesion assays.

Peptide 4D displays the barrier-protecting effect on endothelial monolayer
Subsequently, we examined whether P4D affects the endothelial barrier permeability (Fig. 5). Transendothelial flux of 40-kDa FITC-dextran was elevated only when P4D was applied immediately (at 0 h) after the HMEC-1 cells were seeded (Fig. 5a). We conclude that P4D prevented de novo formation of TJs without disrupting the pre-existing ones. The effect of P4D on endothelial barrier was monitored by the Real-Time Cell Analysis (RTCA). The P4D did not affect the endothelial permeability when applied ~ 24 h after the cell seeding or 24 h after the cytokine treatment (Fig. 5b,  c). Therefore, we treated the HMEC-1 monolayer with P4D, Scr, or FSK 2.5 h after plating when the cells adhered to the bottom of the wells without forming a confluent monolayer, as demonstrated by the low CI levels (Fig. 5d, e). Presumably, at this time period, the TJs have not fully developed and only a minor fraction of F11R/JAM-A molecules have formed trans-homophilic interactions. The endothelium was treated with inflammatory cytokines ~ 60 h later, during the logarithmic growth phase (Fig. 5d, f). The cells from 'P4D & TNF/IFN' sample were retreated with P4D concurrently with TNF/IFN treatment. The barrier-protecting effect of P4D was more evident than that of FSK, when P4D pretreatment was followed by the second supplementary dose applied simultaneously with the cytokines (Fig. 5d, f). Otherwise, P4D did not reveal any barrier-protecting properties without the supplementary dose (Fig. 5f).

Discussion
Our studies on the murine 4T1 breast cancer model demonstrated that administration of Tβ4 and TGF-β1 decreased the sJAM-A levels in murine blood. As the F11R mRNA level in HMEC-1 cells did not change, these observations suggest the reduced "shedding" of the F11R/JAM-A protein from the endothelial cell surface to the blood [38], but not downregulated protein expression [20]. F11R/JAM-A shedding occurs predominantly upon inflammation, when sJAM-A limits the leukocyte recruitment to inflammation sites [38]. The reduced shedding of F11R/JAM-A and decrease in protein expression could result from TGF-β1-induced lysosomal degradation of F11R/JAM-A [39]. Tβ4 probably induced the lysosomal proteolysis of F11R/ JAM-A in a similar mode to TGF-β1.
The lowered F11R/JAM-A expression in MDA-MB-231 cells as compared with two other MEC lines (Fig. 4a) is in accordance with the previously reported negative correlation of JAM-A expression with the metastatic potential of breast cancer cells [19,20].
Decreased plasma level of sJAM-A was suspected to promote the adhesive interactions of breast cancer cells with endothelium. Adhesion is a substantial early step of TEM [4,14]. Moreover, inflammatory cytokines increase the leukocyte adhesion to endothelium, thus triggering F11R-dependent TEM [40]. Consequently, we employed the F11R/JAM-A antagonistic peptide 4D [31,32] that blocked the breast cancer cell adhesion to the inflamed endothelium, which was particularly evident for MDA-MB-231 cells (Fig. 4a). We (Fig. 2a) and other authors [19,20] have shown that this cell line expresses low JAM-A levels as compared with other MECs. Thus MDA-MB-231 cells could be more sensitive to the function of P4D. Migratory ability of MDA-MB-231 cells may be increased as compared with MCF-7 cells due to the lowered level of F11R/JAM-A [19][20][21]. The strongest P4D-dependent reduction of cytokine-stimulated TEM was observed for high JAM-A expressing MCF-7 cells (Fig. 4b). This negates the inverse relation between the JAM-A expression and breast cancer cell motility [19][20][21] and confirms that JAM-A drives the breast cancer cell migration [22][23][24][25]. Moreover, P4D inhibited the Tβ4-induced TEM of breast cancer cells (Fig. 4b). The upregulated TEM of MCF-10A cells confirms that these cells may not represent a perfect model for non-tumorigenic mammary epithelium [41].
P4D abrogated the TJs formation without the endothelial monolayer breakdown (Fig. 5a). The barrier-protecting effect of P4D was enhanced when P4D was applied shortly after the cytokine treatment and P4D administration was repeated with a booster dose (Fig. 5b-f). Concurrently, the inflammatory cytokines enhanced the endothelial permeability (Fig. 5c). Accordingly, TNF-α increased the endothelial permeability, while F11R/JAM-A was removed from TJs and/or internalized [42]. Furthermore, TNF-α with TGF-β3 significantly accelerated the JAM-A internalization [43].
F11R/JAM-A derived peptides were previously applied for the drug development in the cardiovascular disorders  [7,10,31,32,44]. Here, we report that Tβ4 and TGF-β1 decrease the plasma levels of sJAM-A in the murine 4T1 model. Soluble F11R/JAM-A inhibits M.Ab.F11induced platelet aggregation and adhesion to the inflamed endothelium [7,10,31] and attenuates the TEM of neutrophils [38]. Thus P4D is able to restore the sJAM-A function. Accordingly, P4D abrogates de novo formation of TJ as demonstrated by the inhibition of breast cancer cell adhesion to the inflamed endothelium and by the suppression of breast cancer cell TEM.
We demonstrate the role of F11R/JAM-A in breast cancer metastasis. Tumor inducers Tβ4 and TGF-β1 decrease the plasma levels of soluble F11R/JAM-A. This upregulates the interactions between the cancer cells and the endothelium leading to metastasis. The decreased level of sJAM-A can be restored by P4D which blocks adhesion and TEM of breast cancer cells. Thus we suggest that P4D can be considered as a blocker of breast cancer cell extravasation. Nevertheless, in vivo and clinical studies are needed to test the effectiveness of P4D as an anti-metastatic drug. was measured with a Transwell ® two-compartment system. HMEC-1 cells were treated with P4D peptide or with Scrambled P4D peptide (Scr) at a concentration of 500 μM at specified periods of time after seeding. Non-treated cells served as a control sample (CTRL). The plot presents the arithmetic mean ± SD (n = 12). Graphs on panels (b-f) present the results of impedance-based real time measurements of HMEC-1 monolayer permeability shown as the time courses of cytokine-induced and compound-induced alterations of CI levels. The cells were treated with the tested cytokines or compounds at the time points marked with arrows. Control cells (CTRL) were left nontreated and the alterations of their CI values are presented with the black line. b HMEC-1 cells were treated with the tested compounds (P4D, Scr, or FSK) ca. 24 h after plating. c HMEC-1 monolayer was subjected to cytokine (TNF/IFN) treatment ca 48 h after seeding and subsequently to compounds treatment ca. 72 h after seeding. d-f About 2.5 h after seeding HMEC-1 cells were subjected to the compounds treatment followed by the cytokine treatment ca. 67 h after plating. e presents the detailed view of CI levels alterations after the compound treatment, whereas (f) emphasizes the effect of cytokines on the changes in CI values after the compound pretreatment for > 60 h. P4D & TNF/IFN: ca. 2.5 h after seeding, the cells were treated with P4D and next ca. 67 h after plating, the cells were subjected to the concurrent treatment with P4D and cytokines the mammary epithelial cell lines and prepared the cells for experiments. MSt performed flow cytometry analysis. MOS participated in the development of F11R/JAM-A derived peptides and reviewed the manuscript. AB participated in the development of F11R derived peptides, provided all the peptides and scientific consultation on the experiments, and critically reviewed the manuscript. MS provided overall direction and oversight of the project and critically reviewed the manuscript. All authors read and approved the final manuscript.
Funding This work was supported by a grant "Prostacyclin, nitric oxide and carbon monoxide-based pharmacotherapy of endothelial dysfunction and platelet activation-a novel strategy to inhibit cancer metastasis" (acronym: METENDOPHA) funded by the National Center for Research and Development (Cracow, Poland) under the Polish Strategic Framework Program STRATEGMED "Prevention practices and treatment of civilization" (grant coordinated by Jagiellonian Center for Experimental Therapeutics, Jagiellonian University, Cracow, Poland), no. STRATEGMED1/233226/11/NCBR/2015. RB received funding for this project from the statutory program of the Medical University of Lodz no. 503/6-171-01/502-64-091. The funding sources had no influence on study design, the collection, analysis and interpretation of data, the preparation of the manuscript and the decision to submit the article for publication.
Data availability Data supporting these results are available from the corresponding author upon request.

Compliance with ethical standards
Ethics approval All animal procedures and protocols were conducted in accordance with the Guide for the Care and Use of Laboratory Animals of the National Animal Care Committee and were approved by the Local Ethical Committee for Animal Research in Lodz (license number 9/LB51/2017 from 06 February 2017).
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