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Jose Baeza-Noci
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Baeza-Noci, J. Ozone as a Chemotherapy. Encyclopedia. Available online: https://encyclopedia.pub/entry/15969 (accessed on 15 November 2024).
Baeza-Noci J. Ozone as a Chemotherapy. Encyclopedia. Available at: https://encyclopedia.pub/entry/15969. Accessed November 15, 2024.
Baeza-Noci, Jose. "Ozone as a Chemotherapy" Encyclopedia, https://encyclopedia.pub/entry/15969 (accessed November 15, 2024).
Baeza-Noci, J. (2021, November 14). Ozone as a Chemotherapy. In Encyclopedia. https://encyclopedia.pub/entry/15969
Baeza-Noci, Jose. "Ozone as a Chemotherapy." Encyclopedia. Web. 14 November, 2021.
Ozone as a Chemotherapy
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This entry is adapted from the peer-reviewed paper 10.3390/ijms222111796

In the last sixty years, publications in reputed journals have shown the preclinical positive effect of ozone gas in cancer cells. However, the translation of these results into clinical practice is far away from success. A comprehensive approach is necessary for this, and oncologists and researchers need guidance from medical specialists with in-depth knowledge of ozone in medicine. In this article, we review the evidence around this question and suggest different potential research lines to those interested in this exciting field.

ozone therapy oncology cancer

1. Introduction

According to 2020 WHO report [1] on global mortality, cancer is the fifth leading cause of death, and it has been increasing in the past 20 years, whereas cardiovascular diseases and infections are decreasing year after year. If we check the leading causes of death by income group (gross product) and their evolution in the past 20 years, we will realize that this trend is common to all income groups, and in the high-income countries, cancer is the third cause of death after heart attack and dementia. In the next years, we will see cancer as the second cause of death. This will be because of two main reasons: the increase in life expectancy—cancer is directly related to aging—and the decrease in risk factors for heart infarction and better treatments for it.

RT and some CT drugs [2] induce cancer cell death by increasing Reactive Oxygen Species (ROS) and free radicals inside tumor cells. Due to the well-known but still mysterious Warburg effect (aerobic glycolysis or aerobic fermentation of glucose) and its consequences [3], the cancer cell has a very delicate adaptation to an increased ROS production, and any external induction of more ROS could break this balance, triggering cell apoptosis. Cancer cell-increased ROS production is due to a greater intake of glucose and the Warburg effect.

ROS have been reported to be tumorigenic, as they increase cell proliferation, survival, and cellular migration. They induce chromosome damages that initiate tumorigenicity and tumor progression by inactivating phosphatase and tensin homolog (PTEN) and tyrosine phosphatases. On the other side, ROS can also produce cell membrane damage and other deleterious effects that lead to cell death [4].

High-impact journals have published during the past sixty years interesting papers supporting the in vivo and in vitro role of ozone (O 3) in inducing direct cancer cell damage in a harmless way for non-cancer cells. However, few clinical articles have been published, and so, there is small evidence-based support for its clinical use in cancer patients.

2. In Vitro Studies

In 1958, Fetner [5] published in Nature the role of ozone gas in inducing chromosome breakages similar to those effects observed with X-ray irradiation and also the additive effect of X-ray and ozone gas in cell culture. Four years later, the same author [6] confirmed his first observations in a new article using a HeLa cell culture (cervical uterine adenocarcinoma).
In 1980, Sweet et al. [7] described in Science how ozone selectively inhibited, in cell cultures, the growth of three different cancer cell lines (breast, lung, and uterus) without affecting nontumor cells; this effect is related to the ozone dosage and possibly explained because of a defective enzymatic pathway in cancer cells related to the reduced glutathione (GSH) respiratory linked system.
Seven years later, a work from Karlic et al. [8] described a cytotoxic effect of ozone on three ovarian carcinoma cell lines but showed no effect in one endometrial carcinoma cell line, using the same ozone dosage. Irradiation (Ra226, Ir192, or Co60) was used alone and in combination with ozone, finding a radiosensitizing effect of ozone. Control normal cells (skin fibroblasts) had no changes, even with ozone and irradiation with Ra226, but they were damaged by Ir192 or Co60.
In 1990, ozone was described by Zanker and Kroczek [9] as having a similar effect to chemotherapeutic drugs by increasing ROS inside culture cells. They also noticed a synergistic or additive effect on 5-fluorouracil (5-FU) in breast cancer and colon cancer cell lines; even more, ozone overcame chemoresistance to 5-FU in cell lines previously resistant. Ozone and 5-FU did not affect glioma cells neither alone nor together.
That year, Washuttl J. et al. [10] demonstrated that ozone induced damage in the respiratory pathway used by cancer cells (ovarian carcinoma) that induced apoptosis; this damage is similar to the one produced by Doxorubicin or Ifosfamide and does not happen in healthy ovarian tissue.
In 2007, Cannizzaro et al. [11] founded a direct effect of ozone in two neuroblastoma cell cultures (SK-N-SH and SK-N-DZ), in which ozone reduced the cell growth or induced cell apoptosis. In SK-N-SH cells, there was a potentiated effect by combining ozone and cisplatin or etoposide but not with gemcitabine. In SK-N-DZ, only ozone could inhibit the growth of cancer cells.
Simoneti et al. [12] described in 2017 a direct cytotoxic effect of ozone in a human colon cancer cell culture and an increased effect of 5-fluorouracil or cisplatin by combining them with ozone.
One year later, Mokhtari et al. [13] checking the use of Cold Plasma-Activated Media (PAM) found that the underlying mechanism of cancer cell cytotoxicity was the generation of ozone because of the PAM. Six cancer cell lines were tested, and the cytotoxic effect was different. Increasing the PAM time application induced more ozone generation and so, more cytotoxicity. The colon cancer line was the less affected one, and breast cancer was the most damaged line. The authors suggest that the ROS generated by ozone trigger signaling pathways involving c-Jun NH2-terminal kinase (JNK) and p38 kinase and promote mitochondrial perturbation, leading to apoptosis.
Other authors [14] have verified that low ozone concentration did not induce any changes in HeLa cell cultures, suggesting that ozone dose may be important to achieve an antitumor effect.
Lately, Li et al. [15] verified that ozone gas on hepatocarcinoma (bel7402 and SMMC7721 cancer cell lines) cell cultures restrains the proliferation and migration potential thanks to the increase of ROS and the NFKβ suppression.
To summarize this section, ozone gas in normal and cancer cell cultures has variable effects: a direct cytotoxic effect on some types of tumors (not all) while not damaging normal cells when used at the same dosage; there is an additive or synergistic effect with RT and some CT drugs, which is probably related to the intracellular increased production of ROS and other free radicals. This increase in intracellular ROS is badly handled by tumor cells but causes no effect in normal cells due to their intact capability of increasing antioxidants.

3. In Vivo Studies

All the experiments developed on animal models [16][17][18][19][20][21][22][23][24] have not used a direct approach in the sense of a direct gas administration into the tumor, as the in vitro model. Ozone has been given through a systemic way (rectal ozone insufflation and intraperitoneal mainly) and does not reach directly the tumor. Instead, secondary messengers, such as 4-hydroxynonenal (4-HNE), H2O2, and lipoperoxides (mainly 9 alpha-hydroxy-hydroperoxide) generated from the Criegee’s reaction between ozone and polyunsaturated fatty acids placed in albumina are distributed in the whole body [25]. These molecules induce a modulation in nuclear factor NRF2, regulating the Antioxidant Response Elements (AREs) [26], modulating the nuclear factor NFKβ that plays a basic role in inflammation and immune response, and increasing inside erythrocytes 2,3-diphosphoglycerate (2,3-DPG) and ATP, originating an enhanced gas exchange both in lungs and in peripheric tissues and an improvement in the blood flow.
All these mechanisms improve immunity [15][16][26] and increase radiosensibility [17][18][19][20][21][22] in some tumors, but they are not the target of this paper.
Only Kuroda’s team [27] has published a study in an animal model (a mouse with rectal cancer tumor-bearing) showing necrosis and the inhibited proliferation effect of an intratumor injection of 1 mL of ozonated water (ozone dissolved in bi-distilled water at concentrations of 20.8, 41.6, 104, and 208 mM in four groups of mice), compared with 1 mL of bi-distilled water and no treatment. They injected 1 mL of ozonated water at a 208 mM concentration subcutaneously, intraperitoneally, and intramuscularly (0.1 mL) for three days. Ozonated water caused no change in healthy tissues. Higher ozone dosage induced more tumoral necrosis without damaging the normal tissue. These results support the in vitro experiences, but more investigation is needed in this area.

4. Clinical Works

The only paper we have found in our suggested line is from Megele et al. [28] that showed increased survival (30.5 months compared with the standard value of 11.9 months) in a series of four patients with recurrent glioblastoma that were treated with re-resection of the tumor (after relapsing) and intratumoral ozone administered monthly through a catheter (5 mL of oxygen–ozone gas at a concentration of 40 μg of ozone per mL of oxygen—a total dose of 200 μg each time), together with the standard protocol of chemotherapy. The patients received a median of 27 (range: 3–44) oxygen–ozone applications. Another patient was treated with ozone just after the first surgery (together, the RT and CT protocols used in all the patients were included in this case series); he is still alive and without recurrence after 53 months. Two side effects were reported; one catheter was removed temporarily because of an infection and another one, in a different patient, was removed because of a hemorrhage.
Other clinical papers, mainly case reports or short case-control series, have suggested a collaborative effect of ozone with RT [29] or CT [16][30]. The oxygenating effect of ozone [31] can increase the radiosensitivity of some tumors, improving the survival rate. The modulation on the immune system induced by ozone [31] may play a role in enhancing the anti-cancer effect of other drugs.

5. Discussion

RT and many CT drugs have an anti-tumor effect mediated by the production of ROS and free radicals in tumor cells. ROS inhibition decreases CT activity [25], and a selective ROS induction increases tumoricidal result [32].
These ROS induce DNA alterations and other signaling molecules that produce cell apoptosis. In vitro studies have compared the anti-tumoricidal ability of ozone-compared to X-ray [5][6] but also to well-known RT procedures, such as irradiation with Ra226, Ir192, or Co60 [8]. Ozone, at the right dosage, seems to induce the same cellular effect without damaging the normal tissue cells [7] because the antioxidant system in these cells can usually handle this injury, whereas cancer cells have an almost exhausted antioxidant capacity. It is interesting to note that ozone has a radio-sensitizing effect when used with some RT protocols in vitro, turning radiosensible tumor cells that were radioresistant [8].
This radio-mimetic effect has been observed also when comparing ozone with some CT drugs, such as 5-FU [9][12], doxorubicin, or ifosfamide [8]. Ozone induces a similar cancer cell damage to that produced by these drugs by increasing ROS in tumor cells [15]. Moreover, there is a potentiated or synergistic effect when using these CT drugs and ozone together [9][11], the same as what we can observe with the above commented RT protocols. This synergistic effect seems to be different according to the diverse CT drugs used [11] (cisplatin, etoposide, or gemcitabine) and may be different on diverse cancer cell lines.
Recent papers, such as the ones from Mokhtari [13] or Li [15], give us more detailed information about the biochemical pathways used by ROS to induce cell apoptosis in cancer cells.
According to this review, not all tumors are equally susceptible to these potential treatments. We have seen that HeLa cell line is damaged [6] or preserved [14] according to the ozone dose.
These RT-like and CT-like effects have been checked in vitro, but in vivo models are very scarce [27]. Kuroda has checked the efficacy and safety of ozonated water in mice at different ozone concentrations without side effects for healthy tissue at the same dose. The only clinical experience from Megele [28] is very interesting but limited. Increasing the survival rate almost three times is an outstanding result but reduced to five patients.
Systemic ozone has a different mechanism of action [16][17][18][19][20][21][22][23][24], as the usual doses have not proved to induce tumoral cell apoptosis. As this helpful way used in some clinical studies has no direct relation with the RT-like or CT-like ozone effect, we will not deepen our study on it. However, thanks to the great antioxidant capability of the normal cells, higher doses of ozone could have a similar effect to topic ozone gas administration to the tumor, causing no harm to rest of the organism. However, no study has been published in this sense.

6. Conclusion

The use of ozone in cancer needs still a lot of preclinical investigation not only by testing more cancer cell lines but also testing different ozone dosages, as we presently know that all cancer cell lines are not equally affected by ozone.

In vivo studies have been mainly devoted to systemic ozone with low doses. It is mandatory to develop more animal studies following Kuroda’s investigational line, or with intratumoral ozone gas injection.

Randomized control trials should be the third step, after deeper preclinical studies have been done. To develop clinical studies, different interventional approaches can be used theoretically to dispense ozone into the tumor: specific arterial embolization, intratumoral injection, and catheterization. As a single application of ozone is not likely to affect all tumor cells, several applications of this gas would be needed to progressively affect all the tumor.

To use ozone as a CT agent in a systemic way, further studies testing the tumor cell reaction to ozone in vivo must be done. Work is warranted in this regard.

References

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