Research – New Theory of Cancer https://www.newtheoryofcancer.com Recent & Emerging Research Elucidations Mon, 11 Nov 2024 01:58:12 +0000 en-US hourly 1 https://wordpress.org/?v=6.7.1 N. Caninum – “Extremely Effective and Non-Toxic Anticancer” Agent https://www.newtheoryofcancer.com/2024/11/11/n-caninum-extremely-effective-and-non-toxic-anticancer-agent/ Mon, 11 Nov 2024 01:57:58 +0000 https://www.newtheoryofcancer.com/?p=650

Exploring Neospora caninum as a Novel Immunotherapy for Cancer Despite significant advancements in cancer treatment, current therapies often come with high costs and severe side effects, highlighting the need for novel, less toxic alternatives. Recently, growing evidence suggests that certain […]

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Exploring Neospora caninum as a Novel Immunotherapy for Cancer

Despite significant advancements in cancer treatment, current therapies often come with high costs and severe side effects, highlighting the need for novel, less toxic alternatives. Recently, growing evidence suggests that certain parasites may have anticancer effects, as researchers observe an inverse relationship between some parasitic infections and tumor growth. Although some parasites can contribute to cancer progression, others appear to counteract it. These organisms may stimulate anticancer effects either by triggering the host’s immune response or by secreting bioactive molecules with therapeutic potential. By activating immune defenses, these parasites may inhibit key processes in cancer development, such as tumor proliferation, angiogenesis, and metastasis.

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Recent research on Neospora caninum, a protozoan parasite known primarily as a livestock pathogen or canine disease, has revealed unexpected potential as a cancer therapeutic. N. caninum is a eukaryotic, intracellular pathogen, which means it can enter and survive within host cells. This intracellular property allows N. caninum to penetrate and interact directly with cancer cells, potentially enhancing its antitumor effects. Being eukaryotic, it could potentially be engineered to carry larger therapeutic payloads than bacterial or viral therapies, enabling more complex therapeutic applications. In a study using a mouse melanoma model (B16F10), N. caninum demonstrated promising antitumor effects through immune activation and tumor cell destruction. With its ability to initiate a strong immune response, N. caninum may represent a complementary or alternative treatment to current conventional therapies.

Key Findings from the Study

The study reveals that N. caninum administration, both intratumorally and subcutaneously, led to notable tumor inhibition in mice. The treatment stimulated increased cytokine production (IL-12, IFN-γ, IL-10, TNF-α, and IL-2) within the tumor microenvironment, contributing to a heightened immune response against melanoma cells. Unlike other therapies, N. caninum didn’t induce tumor cell death through apoptosis but may exert a direct lytic effect on cancer cells.

In addition to influencing tumor growth directly, N. caninum treatment had subtle yet observable effects on the gut microbiome of treated mice. The findings suggest a shift toward probiotic bacteria such as Lactobacillus, which is associated with enhanced immune activity. This raises the possibility of a dual mechanism where N. caninum supports antitumor immunity both directly within the tumor microenvironment and indirectly by modifying gut microbiota.

Comparing Neospora caninum Therapy to Conventional Cancer Treatments

To understand N. caninum’s place within the current landscape of cancer therapies, we need to consider both its strengths and limitations compared to established methods such as chemotherapy, targeted therapy, and immune checkpoint inhibitors.

AspectNeospora caninum TherapyConventional Cancer Therapies
Mechanism of ActionStimulates immune response, promotes T-cell infiltration, and may directly lyse tumor cells.Chemotherapy: Cytotoxic effect on rapidly dividing cells; Immune checkpoint inhibitors: Unleash T-cell response by blocking inhibitory pathways.
Effect on Tumor MicroenvironmentConverts “cold” tumors into “hot” tumors with inflammatory TME.Varies widely; immune checkpoint inhibitors can also ‘heat up’ the TME but depend on prior T-cell presence.
Safety ProfileGenerally non-pathogenic to humans, although long-term effects need more study.Well-studied safety profiles, though adverse effects can be severe and dose-dependent.
Application MethodBoth intratumoral and subcutaneous injections show efficacy.Typically systemic administration, though localized treatments like intratumoral injections are emerging for certain cancers.
Adverse EffectsMinimal observed in animal studies; theoretically controllable with antimicrobial agents if pathogenicity arises.Immune checkpoint inhibitors: Autoimmune side effects; Chemotherapy: Systemic toxicities affecting multiple organs.
EfficacyDemonstrated tumor inhibition in murine melanoma models, especially with immune enhancement.Efficacy varies based on cancer type and individual response; chemotherapy shows high initial efficacy but also high recurrence.
Impact on Gut MicrobiotaAlters gut microbiome composition; increases beneficial Lactobacillus levels.Immune checkpoint inhibitors and certain targeted therapies can impact gut microbiota but usually not therapeutically.
LimitationsRequires further study in human models; pathogen persistence risk.High recurrence rates, systemic side effects, and often costly for patients.

Strengths and Weaknesses of Neospora caninum as a Cancer Therapy

Strengths: Neospora caninum appears to effectively “warm up” the tumor microenvironment, transforming it into an inflammatory state conducive to antitumor immunity. This immune activation mirrors, to some degree, the effects achieved by immune checkpoint inhibitors. Furthermore, the treatment’s favorable safety profile and minimal adverse effects make it a compelling candidate for patients who have exhausted conventional options.

Weaknesses: N. caninum is still in preclinical stages, with efficacy only demonstrated in animal models. Additionally, as a live microorganism, there is a potential risk of pathogen persistence, especially in immunocompromised patients. A robust understanding of N. caninum‘s interactions with human cells and its long-term effects will be critical before clinical application.

Conclusion

The study of Neospora caninum represents a novel approach in cancer therapy, where immunostimulation and microbiota modulation work together to combat tumor growth. While challenges remain in translating these findings to clinical practice, N. caninum may one day offer oncologists a low-toxicity option for patients resistant to conventional therapies. Further research will determine whether this unconventional therapy can meet the rigorous standards required for human cancer treatment.

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Neospora caninum, a Protozoan Killing Dogs, “Might Be Key” to “Total Regression of Tumors” https://www.newtheoryofcancer.com/2024/05/17/neospora-caninum-a-protozoan-killing-dogs-might-be-key-to-total-regression-of-tumors/ Fri, 17 May 2024 19:54:02 +0000 https://www.newtheoryofcancer.com/?p=153

Neosporosis, caused by the intracellular parasite Neospora caninum, presents a significant challenge in veterinary medicine, leading to serious and life-threatening neurological issues in dogs, and costing the industrial cattle industry billions each year. N. caninum does not infect humans, making […]

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Neosporosis causes paralysis and death in canines. This dog’s symptoms began in the hind legs, requiring a wheelchair for mobility.

Neosporosis, caused by the intracellular parasite Neospora caninum, presents a significant challenge in veterinary medicine, leading to serious and life-threatening neurological issues in dogs, and costing the industrial cattle industry billions each year. N. caninum does not infect humans, making it a potentially safe therapeutic agent.

The study, “Neospora caninum: a new class of biopharmaceuticals in the therapeutic arsenal against cancer“, published in the Journal for ImmunoTherapy of Cancer in 2020, brought to light the game-changing potential of N. caninum in cancer therapy.

The study reported N. caninum effectively destroyed cancer cells and stimulated the immune system to fight tumors. In experiments using a mouse model of thymoma (a type of cancer that affects the thymus gland), researchers observed that injections of live N. caninum tachyzoites, either directly into the tumor or at a distant site, led to significant tumor regression and, in many cases, complete eradication.

Unleashing the Power of the Immune System

The study’s findings point to several key mechanisms by which N. caninum exerts its anti-cancer effects:

  • Direct Cytotoxic Activity: The researchers observed that N. caninum tachyzoites can directly infect and kill cancer cells.
  • Immune System Activation: N. caninum effectively stimulates the immune system, prompting the recruitment of immune cells to the tumor site, effectively transforming what would normally be “cold” tumors (tumors that are not infiltrated by immune cells) into “hot” tumors (tumors that are heavily infiltrated by immune cells).
  • Reprogramming the Tumor Microenvironment: N. caninum alters the tumor’s microenvironment, reducing the presence of immunosuppressive factors that can hinder the immune system’s ability to fight cancer.

The study also highlights the critical role of natural killer (NK) cells, CD8+ T cells, and macrophages in the N. caninum-mediated anti-tumor response. Depleting these immune cell populations through specific antibodies completely abolished N. caninum‘s antitumor activity, underscoring their importance in the process.

NC = Neospora caninum (included a “distant” test)

Advantages Over Existing Therapies

The researchers contrasted N. caninum‘s potential as a cancer therapeutic with the limitations of currently available agents, such as viruses and bacteria, which are sometimes associated with toxicity and safety concerns.

The study authors emphasized these advantages of N. caninum:

  • Safety: Unlike viruses and bacteria that can persist in the body and potentially cause harm, N. caninum is naturally cleared from the system after initiating an immune response, making it a safer alternative.
  • Targeting Efficiency: N. caninum exhibits a remarkable ability to penetrate tumors and cancer cells. This is attributed to its unique apical complex, a specialized structure that allows it to effectively invade a wide range of cell types.
  • Genetic Engineering Potential: N. caninum has a large genome capacity, meaning it can be genetically engineered to carry therapeutic payloads. This opens up possibilities for creating “armed” strains that can deliver additional anti-cancer agents directly to tumor cells.

Promising Results with Human Tumor Model

To further explore the potential of N. caninum for treating human cancers, researchers conducted experiments using a mouse model of Merkel cell carcinoma (MCC), a rare and aggressive form of skin cancer. The results were highly encouraging, demonstrating that treatment with N. caninum led to a significant regression of MCC tumors.

Engineering an Enhanced Strain: NC1-IL15hRec

Recognizing the need for even more potent anti-tumor responses, particularly in advanced or refractory cancers, the researchers engineered a strain of N. caninum called NC1-IL15hRec. This strain secretes a human form of interleukin-15 (IL-15), a cytokine that plays a crucial role in stimulating the immune system, particularly NK cells and CD8+ T cells.

Experiments showed that NC1-IL15hRec induced a robust increase in the proliferation and activity of human immune cells. When tested in the mouse model of thymoma, NC1-IL15hRec exhibited superior anti-tumor efficacy compared to the unmodified strain, demonstrating the potential of enhancing N. caninum‘s therapeutic properties through genetic engineering.

A New Frontier in Cancer Immunotherapy

This study represents a significant step forward in the development of novel cancer treatments that harness the power of the immune system. The findings suggest that N. caninum holds immense promise as a new weapon in the fight against cancer. Further research is ongoing to fully unlock its therapeutic potential and bring this innovative approach to the clinic.

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Hydrogen Therapy: A Promising New Treatment for Lung Cancer https://www.newtheoryofcancer.com/2024/04/28/hydrogen-therapy-a-promising-new-treatment-for-lung-cancer/ Sun, 28 Apr 2024 03:51:36 +0000 https://www.newtheoryofcancer.com/?p=225

Hydrogen inhalation therapy - an emerging therapy for lung cancer, appears to be both safe and effective.

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Recent veterinary & human studies are promising

Sources: “A Systematic Review of Molecular Hydrogen Therapy in Cancer Management“, Asian Pac J Cancer Prev. 2023; 24(1): 37–47
Second era of molecular-targeted cancer therapies in dogs“, J Vet Med Sci. 2023 Aug; 85(8): 790–798

Lung cancer is a leading cause of death worldwide, but recent research has shown that hydrogen therapy may be a promising new treatment. Hydrogen is a colorless, odorless gas that is found in small amounts in the air we breathe. It has been shown to have several benefits for lung cancer patients, including:

  • Reducing tumor growth
  • Improving survival rates
  • Alleviating side effects of chemotherapy and radiation therapy

How Does Hydrogen Therapy Work?

Hydrogen gas is thought to work by reducing oxidative stress, which is a major contributor to cancer development. Oxidative stress occurs when there is an imbalance between the production of free radicals and the body’s ability to neutralize them. Free radicals are unstable molecules that can damage cells and DNA, leading to cancer.

Hydrogen gas has been shown to scavenge free radicals and protect cells from damage. It can also improve the function of the mitochondria, which are the energy-producing units of cells. This can help to slow the growth of cancer cells and improve the overall health of lung cancer patients.

What is the Evidence for Hydrogen Therapy in Lung Cancer?

There is a growing body of evidence to support the use of hydrogen therapy for lung cancer. A number of studies have shown that hydrogen gas can reduce tumor growth and improve survival rates in animal models of lung cancer.

One study, published in the journal Nature Medicine, found that hydrogen gas inhalation reduced tumor growth by 50% in mice with lung cancer. The study also found that hydrogen gas improved the survival rate of the mice by 30%.

Another study, published in the journal Cancer Research, found that hydrogen gas inhalation improved the survival rate of mice with lung cancer by 25%. The study also found that hydrogen gas reduced the side effects of chemotherapy and radiation therapy, such as fatigue, nausea, and vomiting.

Is Hydrogen Therapy Safe?

Hydrogen therapy is generally considered to be safe. It is a non-invasive treatment that does not require surgery or medication. There have been a few reports of side effects, such as headache and fatigue, but these side effects are usually mild and temporary.

Where Can I Get Hydrogen Therapy?

Hydrogen therapy is available at a number of clinics and hospitals around the world. It is typically administered through inhalation, but it can also be taken orally or topically.

The Future of Hydrogen Therapy for Lung Cancer

Hydrogen therapy is a promising new treatment for lung cancer. It is a safe and effective treatment that can reduce tumor growth, improve survival rates, and alleviate the side effects of chemotherapy and radiation therapy. As more research is conducted, hydrogen therapy is likely to become an increasingly important part of the treatment of lung cancer.

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A fitness landscape instability governs the morphological diversity of tip-growing cells https://www.newtheoryofcancer.com/2024/04/22/a-fitness-landscape-instability-governs-the-morphological-diversity-of-tip-growing-cells/ Mon, 22 Apr 2024 22:14:33 +0000 https://www.newtheoryofcancer.com/?p=193 Ohairwe et al. demonstrate that an intrinsic mechanical instability in the convergent mechanism of “inflationary” cell growth shared by diverse tip-growing cells leads to a bifurcation (branching) of their fitness landscape. This bifurcation strictly constrains natural tip-growing cell shapes.

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Ohairwe et al. demonstrate that an intrinsic mechanical instability in the convergent mechanism of “inflationary” cell growth shared by diverse tip-growing cells leads to a bifurcation (branching) of their fitness landscape. This bifurcation strictly constrains natural tip-growing cell shapes.

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Genomic deletions explain the generation of alternative BRAF isoforms conferring resistance to MAPK inhibitors in melanoma https://www.newtheoryofcancer.com/2024/04/22/genomic-deletions-explain-the-generation-of-alternative-braf-isoforms-conferring-resistance-to-mapk-inhibitors-in-melanoma/ Mon, 22 Apr 2024 22:14:32 +0000 https://www.newtheoryofcancer.com/?p=191 Aya et al. show that the production of alternative BRAF mRNA isoforms (altBRAFs), associated with resistance to BRAF inhibitors in melanoma, is caused by genomic deletions rather than by alternative splicing, as previously thought. They also find that altBRAFs are present […]

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Aya et al. show that the production of alternative BRAF mRNA isoforms (altBRAFs), associated with resistance to BRAF inhibitors in melanoma, is caused by genomic deletions rather than by alternative splicing, as previously thought. They also find that altBRAFs are present in treatment-naive, non-V600 BRAF-mutant and BRAF wild-type mutant tumors.

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The soil microbiome modulates the sorghum root metabolome and cellular traits with a concomitant reduction of Striga infection https://www.newtheoryofcancer.com/2024/04/22/the-soil-microbiome-modulates-the-sorghum-root-metabolome-and-cellular-traits-with-a-concomitant-reduction-of-striga-infection/ Mon, 22 Apr 2024 22:14:32 +0000 https://www.newtheoryofcancer.com/?p=192 The soil microbiome protects sorghum, and likely other crops, from infection with the root parasite Striga hermonthica. Kawa et al. show that soil-borne bacteria modify sorghum root development and root exudate content, likely preventing Striga from penetrating sorghum. This study provides […]

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The soil microbiome protects sorghum, and likely other crops, from infection with the root parasite Striga hermonthica. Kawa et al. show that soil-borne bacteria modify sorghum root development and root exudate content, likely preventing Striga from penetrating sorghum. This study provides a framework for developing microbial-based solutions for Striga infestation.

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The nociceptive activity of peripheral sensory neurons is modulated by the neuronal membrane proteasome https://www.newtheoryofcancer.com/2024/04/22/the-nociceptive-activity-of-peripheral-sensory-neurons-is-modulated-by-the-neuronal-membrane-proteasome/ Mon, 22 Apr 2024 22:14:31 +0000 https://www.newtheoryofcancer.com/?p=190 Proteasomes are critical for sensory neuron function. Villalón Landeros et al. uncover a specialized proteasome in somatosensory neurons called the neuronal membrane proteasome (NMP). The NMP mediates crosstalk between somatosensory neurons to modulate sensitivity to stimulation. Inhibition of the NMP reduces […]

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Proteasomes are critical for sensory neuron function. Villalón Landeros et al. uncover a specialized proteasome in somatosensory neurons called the neuronal membrane proteasome (NMP). The NMP mediates crosstalk between somatosensory neurons to modulate sensitivity to stimulation. Inhibition of the NMP reduces sensitivity to mechanical and painful stimuli in vivo.

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Environmentally dependent and independent control of 3D cell shape https://www.newtheoryofcancer.com/2024/04/22/environmentally-dependent-and-independent-control-of-3d-cell-shape/ Mon, 22 Apr 2024 22:14:30 +0000 https://www.newtheoryofcancer.com/?p=188 Using high-throughput light-sheet microscopy, Dent et al. study 3D cancer cell morphogenesis. Environmental cues modulate the opposing roles of non-muscle myosin II (myosin) and microtubules, with varied impacts on RhoGEFs FARP1 and TIAM2. The study underscores the critical interplay between cytoskeletal […]

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Using high-throughput light-sheet microscopy, Dent et al. study 3D cancer cell morphogenesis. Environmental cues modulate the opposing roles of non-muscle myosin II (myosin) and microtubules, with varied impacts on RhoGEFs FARP1 and TIAM2. The study underscores the critical interplay between cytoskeletal regulators and the microenvironment, enhancing our understanding of cell behavior in diverse settings.

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Distributed X chromosome inactivation in brain circuitry is associated with X-linked disease penetrance of behavior https://www.newtheoryofcancer.com/2024/04/22/distributed-x-chromosome-inactivation-in-brain-circuitry-is-associated-with-x-linked-disease-penetrance-of-behavior/ Mon, 22 Apr 2024 22:14:30 +0000 https://www.newtheoryofcancer.com/?p=189 Szelenyi et al. demonstrate that adult brain XCI is systematically biased toward maternal X-active cells, which is sufficient for disease penetrance of the X-linked Fmr1-KO allele. Furthermore, local XCI mosaicism distinguishes phenotypic outcomes of individuals based on mutant X-active cells populating […]

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Szelenyi et al. demonstrate that adult brain XCI is systematically biased toward maternal X-active cells, which is sufficient for disease penetrance of the X-linked Fmr1-KO allele. Furthermore, local XCI mosaicism distinguishes phenotypic outcomes of individuals based on mutant X-active cells populating distinct brain circuits.

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Antibodies targeting the shared cytokine receptor IL-1 receptor accessory protein invoke distinct mechanisms to block all cytokine signaling https://www.newtheoryofcancer.com/2024/04/22/antibodies-targeting-the-shared-cytokine-receptor-il-1-receptor-accessory-protein-invoke-distinct-mechanisms-to-block-all-cytokine-signaling/ Mon, 22 Apr 2024 22:14:29 +0000 https://www.newtheoryofcancer.com/?p=187 Fields et al. demonstrate the viability of targeting a shared cytokine receptor for comprehensive signaling blockade of all associated cytokines. CAN10 and 3G5, two anti-IL-1RAcP antibodies, target distinct epitopes on this shared receptor and potently block IL-1α, IL-1β, IL-33, IL-36α, IL-36β, […]

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Fields et al. demonstrate the viability of targeting a shared cytokine receptor for comprehensive signaling blockade of all associated cytokines. CAN10 and 3G5, two anti-IL-1RAcP antibodies, target distinct epitopes on this shared receptor and potently block IL-1α, IL-1β, IL-33, IL-36α, IL-36β, and IL-36γ signaling.

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