Transcutaneous carbon dioxide application suppresses bone destruction caused by breast cancer metastasis

  • Authors:
    • Toshiyuki Takemori
    • Teruya Kawamoto
    • Takeshi Ueha
    • Mitsunori Toda
    • Masayuki Morishita
    • Etsuko Kamata
    • Naomasa Fukase
    • Hitomi Hara
    • Shuichi Fujiwara
    • Takahiro Niikura
    • Ryosuke Kuroda
    • Toshihiro Akisue
  • View Affiliations

  • Published online on: July 30, 2018     https://doi.org/10.3892/or.2018.6608
  • Pages: 2079-2087
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Abstract

Hypoxia plays a significant role in cancer progression, including metastatic bone tumors. We previously reported that transcutaneous carbon dioxide (CO2) application could decrease tumor progression through the improvement of intratumor hypoxia. Therefore, we hypothesized that decreased hypoxia using transcutaneous CO2 could suppress progressive bone destruction in cancer metastasis. In the present study, we examined the effects of transcutaneous CO2 application on metastatic bone destruction using an animal model. The human breast cancer cell line MDA-MB-231 was cultured in vitro under three different oxygen conditions, and the effect of altered oxygen conditions on the expression of osteoclast-differentiation and osteolytic factors was assessed. An in vivo bone metastatic model of human breast cancer was created by intramedullary implantation of MDA-MB-231 cells into the tibia of nude mice, and treatment with 100% CO2 or a control was performed twice weekly for two weeks. Bone volume of the treated tibia was evaluated by micro-computed tomography (µCT), and following treatment, histological evaluation was performed by hematoxylin and eosin staining and immunohistochemical staining for hypoxia-inducible factor (HIF)-1α, osteoclast-differentiation and osteolytic factors, and tartrate-resistant acid phosphatase (TRAP) staining for osteoclast activity. In vitro experiments revealed that the mRNA expression of RANKL, PTHrP and IL-8 was significantly increased under hypoxic conditions and was subsequently reduced by reoxygenation. In vivo results by µCT revealed that bone destruction was suppressed by transcutaneous CO2, and that the expression of osteoclast-differentiation and osteolytic factors, as well as HIF-1α, was decreased in CO2-treated tumor tissues. In addition, multinucleated TRAP-positive osteoclasts were significantly decreased in CO2-treated tumor tissues. Hypoxic conditions promoted bone destruction in breast cancer metastasis, and reversal of hypoxia by transcutaneous CO2 application significantly inhibited metastatic bone destruction along with decreased osteoclast activity. The findings in this study strongly indicated that transcutaneous CO2 application could be a novel therapeutic strategy for treating metastatic bone destruction.

Introduction

Breast cancer is the primary cause of cancer mortality in women (1), with bones among the most common metastatic sites (2,3). Bone metastasis increases skeletal-related events (SREs), which are defined as pathological fractures, spinal cord compression and bone pain requiring palliative radiotherapy and/or surgical treatment, and worsens the activities of daily living and patient quality of life. Bone destruction associated with cancer metastasis is caused by activated osteoclast function, but not by the direct effects of cancer cells in the bone (4). For osteoclast activity, receptor activator of nuclear factor κ-B ligand (RANKL) promotes osteoclast differentiation, formation and bone-resorptive ability by binding to its receptor, RANK, which is expressed in both hematopoietic osteoclast-precursor cells and mature osteoclasts. In the area of bone metastasis, cancer cells produce several osteolytic factors, including parathyroid-hormone-related peptide (PTHrP), interleukin (IL)-1β, IL-6 and IL-8, each of which can stimulate osteoblasts and/or stromal cells to increase RANKL expression (57). Additionally, RANKL is also expressed in metastatic cancer cells (8,9), with its overexpression in the area of bone metastasis inducing osteoclast activation (10). Recently, osteoclast function was focused on as a therapeutic target in metastatic bone tumors, and several inhibitors of osteoclast activity, such as bisphosphonates and denosumab, have been developed and used to prevent metastatic bone destruction. However, the effects of these treatment modalities remain limited. In addition, osteonecrosis of the jaw and hypocalcemia represent serious side-effects and long-term prognosis associated with these treatments remains unknown (1114).

Hypoxia is a common feature of malignant tumors, including metastatic bone tumors. Tumor hypoxia is caused by an inadequate supply of oxygen that occurs when the tumor outgrows its blood supply, resulting in chronic hypoxia and the inability of oxygen to reach some cells due to the large diffusion distance (1517). Hypoxia strongly contributes to the reduced efficacy of certain chemotherapeutic agents and/or radiotherapy and represents a major cause of tumor propagation (15,16,18). Additionally, tumor-associated hypoxia plays a significant role in tumor progression associated with bone metastasis (19,20). Hypoxic conditions allow factors, such as hypoxia-inducible factor-1 (HIF-1), to overexpress and trigger the production of angiogenic proteins (17,21,22). HIFs are essential factors for maintaining cellular oxygen homeostasis and adaptation to hypoxic environments. HIF-1α, an oxygen-dependent α subunit of HIF (23), is activated by hypoxia and induces RANKL expression. Increased hypoxia accompanied by HIF-1 overexpression also promotes the progression of bone metastasis in breast cancer (24,25). Therefore, tumor hypoxia can be considered as an attractive therapeutic target involved with bone metastases.

To obtain local oxygenation in tumor tissues, a direct absorption of oxygen through the skin can be considered, however oxygen is not easily absorbed through the skin (26). We previously demonstrated that transcutaneous CO2 application could lead to increased oxygen release from red blood cells, known as a physiological phenomenon, the Bohr effect (27,28). Oxygenation in treated tissues could be easily and effectively induced by the transcutaneous CO2 treatment via the oxygen dissociation from hemoglobins (28). Using the CO2 treatment, we could induce mitochondrial apoptosis in human cancer xenografts and improve hypoxia in cancer tissues in the absence of side-effects (2932). Based on these findings, we hypothesized that hypoxia would promote bone destruction via the activation of factors related to osteoclast differentiation and osteolysis, and that recovery from hypoxia following transcutaneous CO2 application would inhibit bone destruction by cancer metastasis. In the present study, we examined whether oxygen conditions affect the expression of osteoclast-differentiation and osteolytic factors in vitro, as well as the effects of recovery from hypoxia following transcutaneous CO2 application on bone destruction and osteoclast activity using an in vivo bone metastatic model of breast cancer.

Materials and methods

Cell lines

The human breast cancer cell line MDA-MB-231 was obtained from the American Type Culture Collection (ATCC; Manassas, VA, USA) (33), and cells were grown as monolayers in Dulbecco's modified Eagle's medium (DMEM; Sigma-Aldrich; Merck KGaA, St. Louis, MO, USA) supplemented with 10% (v/v) fetal bovine serum (FBS; Sigma-Aldrich; Merck KGaA), 100 U/ml penicillin and 100 µg/ml streptomycin. The cultures were maintained in a humidified atmosphere with 5% CO2 at 37°C.

In vitro experiments

To investigate the effect of altered oxygen conditions on breast cancer cells in vitro, MDA-MB-231 cells were incubated for 6 days in one of three different oxygen conditions: normoxic (20% O2, 5% CO2), hypoxic (2% O2, 5% CO2) or reoxygenated conditions. For the reoxygenated condition, cells were incubated under normoxic conditions (20% O2, 5% CO2) for 3 days followed by 3 days of incubation under hypoxic conditions (2% O2, 5% CO2), as previously described (30,32). Following incubation, total RNA was collected from the cells and the mRNA levels of RANKL, PTHrP, IL-1β, IL-6 and IL-8 were evaluated by quantitative real-time polymerase chain reaction (qPCR).

Animal models

Female BALB/c nude mice aged 5 weeks old were obtained from CLEA Japan Inc. (Tokyo, Japan). Animals were maintained under pathogen-free conditions in accordance with institutional guidelines. Animals were fed pathogen-free laboratory chow and allowed free access to autoclaved water in an air-conditioned room with a 12-h light/dark cycle. All animal experiments were approved by the Ethics Committee of the Kobe University Animal Experimentation Regulations (permission no. P120404-R1). To create the in vivo bone metastasis model of breast cancer, 18 mice were randomly divided into two groups: a CO2-treated group (CO2 group; n=9) and a control group (n=9). MDA-MB-231 cells [1.0×106 cells in 10 µl phosphate-buffered saline (PBS)] were intramedullary implanted into the proximal epiphysis of the tibia of all mice in both groups (34). For surgical procedures, mice were anesthetized by intraperitoneal injection of 20–30 mg/kg pentobarbital sodium for induction and isoflurane inhalation at a concentration of 2% for maintenance.

Transcutaneous CO2 application

Transcutaneous CO2 application was performed as previously described (3032,35). Briefly, the area of skin around the lower limb where MDA-MB-231 cells were implanted was treated with CO2 hydrogel. This area was then sealed with a polyethylene bag, and 100% CO2 gas was administered into the bag. Mice in the control group were treated similarly, replacing CO2 with room air.

In vivo studies

Examination of the in vivo effects of transcutaneous CO2 application on breast cancer bone metastasis was performed following treatment (CO2 or air) at 4-week post-implantation of MDA-MB-231 cells and for 10 min/mouse, twice weekly for 2 weeks. The tumor volume and body weight were monitored twice weekly until the end of the treatment. Tumor volume was calculated as previously described according to the formula V = π/6 × a2 × b, where a and b represent the shorter and longer diameters of the tumor cell implanted proximal tibia, respectively (36).

qPCR analysis

Total RNA was extracted from cells and tumor tissues by selective binding to a silica-gel-based membrane using an RNeasy mini kit according to the manufacturer's protocol (Qiagen, Valencia, CA, USA). Oligo (dT)-primed first-stand cDNA was synthesized using a high-capacity cDNA transcription kit (Applied Biosystems, Foster City, CA, USA). qPCR was performed in a 20-µl reaction mixture using SYBR Green Master Mix reagent (Applied Biosystems; Thermo Fisher Scientific, Inc., Foster City, CA, USA) on an ABI Prism 7500 sequence-detection system (Applied Biosystems; Thermo Fisher Scientific, Inc.). PCR conditions were as follows: one cycle at 95°C for 10 min, followed by 40 cycles at 95°C for 15 sec and 60°C for 1 min. Pre-designed primers specific for RANKL, PTHrP, IL-1β, IL-6 and IL-8 were obtained from Invitrogen Life Technologies; Thermo Fisher Scientific, Inc. (Carlsbad, CA, USA). Primer sequences were as follows: RANKL forward, 5′-CCCAGATCAAGGTGGTGTCT-3′ and reverse, 5′-TGCTGACCAATGAGAGCATC-3′; PTHrP forward, 5′-CATCAGCTCCTCCATGACAA-3′ and reverse, 5′-TCAGCTGTGTGGATTTCTGC-3′; IL-1β forward, 5′-GGACAAGCTGAGGAAGATGC-3′ and reverse, 5′-TCGTTATCCCATGTGTCGAA-3′; IL-6 forward, 5′-AAAGAGGCACTGGCAGAAAA-3′ and reverse, 5′-TTTCACCAGGCAAGTCTCCT-3′; IL-8 forward, 5′-GTTCCACTGTGCCTTGGTTT-3′ and reverse, 5′-GCTTCCACATGTCCTCACAA-3′. Relative expression of RANKL, PTHrP, IL-1β, IL-6 and IL-8 was calculated using the ∆∆Cq method (37), with normalization against β-actin levels.

Micro-computed tomography (µCT) analysis

Quantitative analysis of treated tibiae was performed both before and after treatment using a µCT Scanner (R_mCT; Rigaku Mechatronics Co., Ltd., Tokyo, Japan). Following the end of treatment, all mice were euthanized by intraperitoneal injection of 1 ml pentobarbital sodium (Kyoritsu Seiyaku, Tokyo, Japan), and the treated tibiae were removed. The bone samples were scanned by µCT, and using the constructed sagittal image from the scanning data, histomorphometric analysis of the proximal epiphysis of the tibia, excluding the cortical bone, was performed. Bone volume was assessed using an image-analysis system (TRI/3D-BON; Ratoc System Engineering, Tokyo, Japan). Following µCT scanning, samples were fixed in 10% formalin for 48 h.

Hematoxylin and eosin (H&E) staining

Formalin-fixed tibia samples were decalcified in 10% ethylenediaminetetraacetic acid for 2 weeks and embedded in paraffin. Paraffin-embedded tibia samples were sliced into 6-µm-thick sections and stained with H&E. Sections were evaluated using a light microscope to confirm bone destruction and the presence of cancer cells.

Immunohistochemical analysis

Paraffin-embedded tibia sections were pretreated with citrate buffer for 40 min at 95°C and quenched with 0.05% H2O2, followed by overnight incubation at 4°C with the following primary antibodies in Can Get Signal Immunostain Solution A (Toyobo, Osaka, Japan): mouse anti-HIF-1α antibody (1:1,000; cat. no. sc-13515; Santa Cruz Biotechnology, Dallas, CA, USA), rabbit anti-RANKL antibody (1:1,000; cat. no. ab9957; Abcam, Tokyo, Japan), rabbit anti-IL-1β antibody (1:1,000; cat. no. ab9722; Abcam), mouse anti-IL-6 antibody (1:1,000; cat. no. sc-130326; Santa Cruz Biotechnology) and mouse anti-IL-8 antibody (1:1,000; cat. no. sc-7303; Santa Cruz Biotechnology). Following washes, the sections were incubated with horseradish peroxidase-conjugated labeled anti-mouse (cat. no. 424131) or anti-rabbit (cat. no. 424141) antibody (1:200; Histofine Simplestain Max PO; Nichirei, Tokyo, Japan) for an additional 30 min at room temperature, counterstained with hematoxylin, and examined with a BZ-X700 confocal microscope (Keyence Corporation, Osaka, Japan). Immunopositive cells were counted in three random fields under a high-power field (×200).

Tartrate-resistant acid phosphatase (TRAP) staining

To evaluate the effect of transcutaneous CO2 treatment on osteoclast activity in metastatic bone tumors, TRAP staining was performed in paraffin-embedded histological sections using the standard naphthol AS-BI phosphate post-coupling method (38). Slides were incubated at 37°C in sodium acetate buffer (pH 5.0) containing 0.01% naphthol AS-BI phosphate and 0.5 Ml- (+) tartaric acid. The sections were then incubated in the same buffer containing pararosaniline chloride for 20 min, followed by washing in distilled water. The sections were counterstained with hematoxylin for 30 sec, dehydrated with alcohol and penetrated with xylene. TRAP-positive multinucleated cells containing more than three nuclei were counted as osteoclasts in three random fields under a light microscopy.

Statistical analysis

All experiments were performed independently in triplicate, and data are presented as the mean ± standard error of the mean (SEM) unless otherwise indicated. Differences between groups were evaluated using the Mann-Whitney U test and also by analysis of variance (ANOVA) with a Tukey's post hoc test to compare continuous values. All tests were considered to indicate a statistically significant difference at P<0.05.

Results

Hypoxic conditions increase mRNA expression of osteoclast-differentiation and osteolytic factors in MDA-MB-231 breast cancer cells in vitro

The mRNA expression of RANKL, PTHrP and IL-8 was significantly increased in cells under hypoxic conditions compared with their expression observed under normoxic conditions (P<0.05), with the elevated expression of the three factors subsequently decreased to the same levels as those under normoxic conditions following reoxygenation (Fig. 1). We also observed elevated expression of IL-1β and IL-6 under hypoxic conditions, however, this increase was not statistically significant (Fig. 1).

Transcutaneous CO2 application suppresses tumor growth and prevents bone destruction in a bone metastatic model of human breast cancer

Transcutaneous CO2 treatment significantly suppressed breast cancer tumor growth compared with that observed in controls (Fig. 2A). In addition, at the end of the experiment, the tumor volume in the CO2 group was 49% of that in the control group (Fig. 2B) (P<0.05). There was no significant difference in body weight between the groups (Fig. 2C).

µCT analyses demonstrated that transcutaneous CO2 application blocked bone destruction compared with the control treatment, and that bone volume was significantly preserved in the CO2 group (Fig. 3A and B). H&E staining of treated tibiae also revealed that the area of cancer tissues in the CO2 group was smaller than that in the control group (Fig. 3C).

Osteoclast activity is significantly inhibited by transcutaneous CO2 application and via decreased expression of osteoclast-differentiation and osteolytic factors along with decreased HIF-1α expression

Immunopositive staining for HIF-1α was weakly detected in CO2-treated tibiae, whereas positive staining was extensively observed in the control tibiae (Fig. 4). For TRAP staining, the number of TRAP-positive multinucleated osteoclasts was significantly reduced following transcutaneous CO2 treatment compared with that observed in the controls (Fig. 5A and B). Additionally, immunohistochemical staining for osteoclast-differentiation and osteolytic factors revealed that staining for RANKL, IL-1β, IL-6 and IL-8 was barely detectable in the CO2-treated tibiae, but was strongly positive in the control group (Fig. 6A). Furthermore, the number of cells immunopositive for these factors in the CO2-treated tumors was significantly decreased compared with that observed in the control tumors (Fig. 6B).

Discussion

In the area of bone metastasis, osteolysis is mainly caused by activated osteoclast function and not by the direct effects of metastatic cancer cells (4,39). In response to factors associated with osteoclast differentiation (RANKL) and osteolysis (PTHrP, IL-1β, IL-6 and IL-8), which are produced by cancer cells, osteoblast-mediated cross-talk between RANKL and its receptor, RANK, which is expressed in hematopoietic osteoclast-precursor cells and mature osteoclasts, is promoted, followed by stimulation of osteoclast activity, especially bone-resorptive functions (57,4042). In particular, PTHrP induced osteoclast formation through the upregulation of RANKL (42) and represented a specific mediator of osteolysis in metastatic breast cancer (43,44). Previous studies reported that breast cancer cells secreted high levels of RANKL, IL-1β and IL-6 under hypoxic conditions (4547). In the present study using MDA-MB-231 breast cancer cells, we observed that the in vitro expression of factors, including RANKL, PTHrP, IL-1β, IL-6 and IL-8, was increased under hypoxic conditions and subsequently decreased by reoxygenation. These findings were consistent with previous studies (4547) and indicated that hypoxic conditions affected the expression of osteoclast-differentiation and osteolytic factors, which play essential roles in bone destruction associated with cancer metastasis. Based on these findings, we hypothesized that improving hypoxia could suppress the stimulation of osteoclast activity, and that recovery from hypoxia would inhibit bone destruction by cancer metastasis.

Hypoxia is a common feature of solid tumors, including metastatic bone tumors, and is mainly a consequence of poor perfusion in solid tumors. In bone metastasis, abnormal blood vessels are insufficient to supply oxygen to metastatic tumor tissues, causing intratumoral hypoxia (48). The median tumor oxygen concentration in breast cancer is reportedly ≤1.3%, which is substantially lower than that in normal tissues (25). Hypoxia negatively affects clinical outcomes, including overall patient survival, motility, and resistance to chemotherapy and/or radiotherapy by impacting tumor-cell functions. The transcription factor HIF-1 is a key regulator of the cellular response promoting survival in the hostile environment of hypoxic tumors (23). In human malignancies, HIFs critically contribute to chemoresistance and/or radioresistance (49) and are associated with histological grade, stage and local or distant recurrence (5053). Recently, a role for HIF-1α in promoting lung and bone metastases was described using a transgenic model of breast cancers (25). Therefore, improvement of hypoxic conditions by regulating HIF-1α in metastatic bone tumors may control not only tumor progression, but also bone destruction. Although several therapeutic strategies to overcome hypoxia and/or to specifically target hypoxic cells have been investigated, attempts to improve tumor oxygen levels have not yielded clinically compelling results (5456), and metastatic bone tumors are still considered an incurable disease. Recent therapeutic strategies for treating bone metastasis include surgery, radiotherapy and osteoclast inhibitors, such as bisphosphonates and denosumab, the human monoclonal antibody used to neutralize RANKL. Regardless of the wide use of these treatments, radiotherapy should still be administered for symptom palliation (57), although bisphosphonates and denosumab can cause unfavorable side-effects, such as osteonecrosis of the jaw (1114). Based on these findings, new strategies for the treatment of bone metastases with fewer side-effects are required.

The benefits of CO2 therapy have been realized for therapeutic purposes, especially in the treatment of peripheral vascular disorders (58), and carbonated spa therapy has historically been used in Europe as an effective treatment for cardiac diseases and skin problems (59,60). The therapeutic effects of CO2 are mediated by an increase in blood flow and microcirculation, nitric oxide-dependent neocapillary formation and an increase in the partial pressure of O2 in local tissue, known as the Bohr effect (27). The Bohr effect is represented by a rightward shift in the O2-hemoglobin dissociation curve accompanied with increased pCO2 or decreased pH (27). We previously demonstrated that transcutaneous CO2 application increased O2 pressure in treated tissues, through the absorption of CO2, potentially causing an artificial Bohr effect (28). Transcutaneous CO2 application suppressed the in vivo human undifferentiated pleomorphic sarcoma/malignant fibrous histiocytoma tumor growth through induction of mitochondrial apoptosis accompanied by mitochondrial proliferation (29). Additionally, animal models of osteosarcoma (30) and oral squamous cell carcinoma (31) demonstrated that CO2 treatment decreased metastatic potential along with decreased expression of both HIF-1α and vascular endothelial growth factor (30,31). These findings strongly indicated that transcutaneous CO2 application exhibited antitumor effects by improving hypoxic conditions within tumor tissues (2931). In the present study, we revealed that transcutaneous CO2 application in a bone metastatic model of human breast cancer, significantly improved intratumoral hypoxia along with decreased expression of HIF-1α, RANKL and osteolytic factors, as well as suppressed osteoclast function along with decreased TRAP activity, resulting in blockage of progressive bone destruction without observable side-effects.

However, the present study had several limitations. Firstly, we have not examined the influence of CO2 application on osteoblasts in the surrounding tissues. We previously reported that CO2 application accelerated fracture repair in a rat-fracture model by increasing osteoblast activity (61). In addition, several studies revealed that, in the presence of osteolytic bone metastasis, tumor cells increased the RANKL production of osteoblasts in the surrounding bone stroma of the host with decreased osteoprotegerin, by releasing a variety of factors including interleukins and PTHrP, resulting in more osteoclast formation and bone degradation (62,63). Based on these previous studies, CO2 application may inhibit the tumor-induced RANKL production of osteoblasts, resulting in decreased bone destruction via decreased osteoclast activity. Secondly, we observed that transcutaneous CO2 application could inhibit metastatic bone destruction along with decreased osteoclast activity in a well-established bone metastatic model using MDA-MB-231 human breast cancer cells, however we used only one breast cancer cell line in the present study. Additionally, we did not directly assess the oxygen conditions in the metastatic bone during transcutaneous CO2 treatment. Therefore, further investigations are required to clarify the effects of transcutaneous CO2 application on cancer cells and bone destruction in metastatic bone tumors. In conclusion, our findings strongly indicated that oxygen conditions affected the expression of osteoclast-differentiation and osteolytic factors, which play essential roles in bone destruction by breast cancer cells, and that transcutaneous CO2 application blocked metastatic bone destruction by improving hypoxic conditions along with decreased expression of osteolytic factors and TRAP activity. Although further studies are required to elucidate the mechanisms associated with the effects of CO2 application, transcutaneous CO2 application can be considered a potential therapeutic strategy for the treatment of metastatic bone destruction in breast cancer patients.

Acknowledgements

We thank Mrs. Minako Nagata, Mrs. Maya Yasuda and Mrs. Kyoko Tanaka for their expert technical assistance. The abstract was presented at the 2018 Annual Meeting of the Orthopaedic Research Society Mar. 10-13, 2018 in New Orleans, LA, USA and was published as abstract no. 2073.

Funding

No funding was received.

Availability of data and materials

The datasets used and analyzed during the current study are available from the corresponding author upon reasonable request.

Authors' contributions

TT, TK, TU, MT, NF, HH, TN, RK and TA conceived and designed the study. TT performed the experiments and wrote the initial draft of the manuscript. TT, TU, MT, MM, SF and EK performed the analyses and interpretation of data. TK is the principal investigator and was involved in the conceptualization, experimental design, discussion of the data, and writing of the manuscript. All authors read and approved the manuscript and agree to be accountable for all aspects of the research in ensuring that the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Ethics approval and consent to participate

All animal experiments were approved by the Ethics Committee of Kobe University Animal Experimentation Regulations (permission no: P120404-R1).

Patient consent for publication

Not applicable.

Competing interests

The hydro-gel was donated from Neochemir, Inc. TU is a full-time employee of Neochemir, Inc. The international patent publication number is WO2004/002393, with a publication date of January 8, 2004. This does not alter the author's adherence to all journal policies on sharing data and materials.

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October-2018
Volume 40 Issue 4

Print ISSN: 1021-335X
Online ISSN:1791-2431

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Copy and paste a formatted citation
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Spandidos Publications style
Takemori T, Kawamoto T, Ueha T, Toda M, Morishita M, Kamata E, Fukase N, Hara H, Fujiwara S, Niikura T, Niikura T, et al: Transcutaneous carbon dioxide application suppresses bone destruction caused by breast cancer metastasis. Oncol Rep 40: 2079-2087, 2018
APA
Takemori, T., Kawamoto, T., Ueha, T., Toda, M., Morishita, M., Kamata, E. ... Akisue, T. (2018). Transcutaneous carbon dioxide application suppresses bone destruction caused by breast cancer metastasis. Oncology Reports, 40, 2079-2087. https://doi.org/10.3892/or.2018.6608
MLA
Takemori, T., Kawamoto, T., Ueha, T., Toda, M., Morishita, M., Kamata, E., Fukase, N., Hara, H., Fujiwara, S., Niikura, T., Kuroda, R., Akisue, T."Transcutaneous carbon dioxide application suppresses bone destruction caused by breast cancer metastasis". Oncology Reports 40.4 (2018): 2079-2087.
Chicago
Takemori, T., Kawamoto, T., Ueha, T., Toda, M., Morishita, M., Kamata, E., Fukase, N., Hara, H., Fujiwara, S., Niikura, T., Kuroda, R., Akisue, T."Transcutaneous carbon dioxide application suppresses bone destruction caused by breast cancer metastasis". Oncology Reports 40, no. 4 (2018): 2079-2087. https://doi.org/10.3892/or.2018.6608