4 Factors and Prevention Strategies For Cancer Metastasis

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Increasing mortality rates associated with cancer metastasis has significantly impacted the cancer research community over the last decade. The spread of cancer is complex and involves a domino effect of influences which promote an environment for cancer cells to thrive.

Cyclic series of events innately drive cancer. Stress leads to cellular damage. Untreated damage creates more inflammation and genetic abnormalities that intensify the ability for cancer to develop. Inflammation breaks down healthy cell signaling allowing cancer cells to form tumors and spread throughout the body (metastasize).

This article will cover the 4 key factors that cause cancer metastasis in the body. You will also learn natural ways to combat these influences from wreaking havoc within your cells and how to detect cancer early.

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Factor 1: Chronic Inflammation

One of the key driving forces behind cancer metastasis is systemic inflammation. It is suspected that chronic inflammation is the primary cause of 25% of all human cancers. Inflammatory conditions contribute to the ability of cancer cells to rapidly grow, form tumors, and even resist cancer treatment drugs.

Inflammation increases tissue damage and is a major cause of epigenetic changes. While scientist once thought that the genes we were given at birth were unchangeable, the field of epigenetics provides evidence that environmental factors we are exposed to (ie. nutrition, toxins, stress) can turn genes off and on causing genetic abnormalities.

Genetic alterations result in the following consequences:

  • Activation of EMT Activity: EMT (epithelial-mesenchymal transition) activity is turned on, triggering a series of pathways that maintain chronic inflammation. EMT pathways boost tumor cell migration by breaking down adhesive anchors to cancers cells, thus increasing their ability to move and invade new tissue.
  • Transcriptional Changes: Many transcription factors that act as on/off switches for the expression of genes are altered under conditions of inflammation. These controlling factors have the ability to repress E-cadherin activity normally responsible for maintaining the adhesive properties that binds a cell to a location.
  • Immune Cell Secretion: Inflammatory cells like lymphocytes and neutrophils infiltrate tumors causing the release of other cellular agents that promote metastasis including cytokines and growth factors.
  • Overexpression of LOX: LOX or lysyl oxidase changes enzymatic activity associated with cellular adhesion. As a result, increased LOX expression induces several of the influences mentioned above including EMT activation and the suppression of E-cadherin activity.

Factor 2: Modified Nrf2 Signaling

Nrf2 (nuclear factor-E2-related factor 2) signaling is involved in numerous functions in the body associated with healing. Nrf2 aids in DNA repair and has anti-inflammatory properties that regulate cellular adhesion. It also regulates enzyme activity and apoptosis and otherwise acts as a super antioxidant defense system.

This transcription factor is intrinsically involved in maintaining homeostasis throughout the body via stress management. Three major stress molecules including reactive oxygen species (ROS), hydrogen peroxide (H202), and reactive nitrogen species (RNS) are toxic to biological systems and are regulated by Nrf2.

Oxidative stressors ultimately degrade Nrf2 preventing its ability to block genetic mutations from occurring while aiding cells to appropriately manage stress.

Factor 3: Secretion of Connective Tissue-Dissolving Enzymes

The overexpression of metalloproteinases or MMPs is indicative of cancer metastasis. MMPs are a family of enzymes that break down the extracellular matrix within a cell. Typically, a healthy cell utilizes this connective network of tissue to communicate with other cells and its environment while also providing structure and various physiological functions.

When this matrix is degraded, there is an increased risk of malignant tumor growth. This is due to increased cellular permeability, response changes to surrounding stimuli including angiogenesis (new blood vessel growth), and increased systemic inflammation. Of the 21 MMPs recognized in the development of chronic conditions and disease, a select few are used as biomarkers in identifying aggressive cancer types.

MMP-13 activity is prevalent in metastatic breast cancers, urinary cancer, as well as skin, head, and neck cancers. MMP-11 is evident in invasive breast and skin cancer. MMP-2 and MMP-9 play a key role in cancer malignancy because they are associated with increasing tumor growth.

Specifically, these MMPs support metastatic growth factors like angiogenesis. They act as traffic controllers sending signals to inflammatory compounds and light the path to receptors. Once MMPs bind to these receptors they activate numerous other metastatic influences.

Factor 4: Angiogenesis

The development of new blood vessels to an abnormal cell naturally promotes aggressive tumor development. Angiogenesis provides a cancer cell with adequate blood flow and nutrients required to invade new tissue.

This energy fuels a tumor to create biological changes once it invades and interacts with endothelial cells. Thin layers of endothelial cells lines blood and lymphatic vessels. Once interaction with these cells is initiated, cancer has the ability to circulate throughout the body and invade distant tissue.

As infection increases and the cancer grows, conditions of hypoxia increases, further inducing LOX and giving rise to a cascade of adverse but favorable conditions to the tumor. Chronic inflammation leads to inflamed cells, prolonged oxidative stress, and the inability of the body to identify and eliminate the infectious cancer growth.

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Cancer Tumor Prevention Strategies

The following strategies will increase the chemoprotective properties of your cells and limit cellular toxicity that stimulates cancer metastasis.

1. Limit MMP Activity

Improving the regulation of MMP activity in cells is essential to reducing the breakdown of connective tissue within a cell and combating cancer metastasis. Some of the best dietary compounds that inhibit MMP activity and promote detoxification in the body are:

  • Polyphenols: EGCG (epigallocatechin-3-gallate) found in green tea, resveratrol in dark grapes and berries, and curcumin-active turmeric
  • Flavonoids: Quercetin, predominantly found in citrus fruits as well as apples
  • Isothiocyanates: Sulfur-containing compounds including sulforaphane concentrated in broccoli and a variety of cruciferous veggies

Incorporating more of these antioxidants into your diet has been shown to effectively treat colon, prostate, kidney, and liver cancer − to name only a few. Simultaneous dietary phytochemicals provide significant cancer protective benefits to healthy cells and create cytotoxic effects to tumor cells. You can also support cellular integrity by consuming foods rich in zinc, magnesium, and vitamin C.

2. Consume an Anti-Inflammatory Diet

Consuming an anti-inflammatory chemopreventive diet is the best way to prevent the aggressive behavior of cancer metastasis. These nutrients inhibit inflammatory enzymes and suppress carcinogenic activity:

  • Berberine: Natural antibiotic with powerful anti-inflammatory properties. Found in goldenseal root and Oregon grape root
  • Luteolin: Suppresses cancer by stimulating enzymes and supports elimination of toxins. Found in chamomile tea, celery, and green peppers
  • Curcumin: Blocks TNF (tumor necrosis factor) therefore decreasing tumor growth activity. Active component in turmeric
  • Kaempferol and Quercetin: Inhibits uric acid synthesis. Abundant in blackberries, spinach, onions, and cucumbers
  • Apigenin: Scavenges free radicals and supports detoxification pathways. Concentrated in onions, oranges, and grapefruit

The key to preventing chronic inflammation and suppressing cancer growth is to limit foods high in sugar and starch. Genetically modified grains have flooded the marketplace and fuel cancer growth by supplying a steady feed of glucose.

Rather than feeding cancer, starve it by consuming foods that help maintain low blood sugar levels. These foods include 100% grass-fed beef and raw cheeses, and organic pasture-raised poultry. Adding low-carb fermented foods and beverages to your diet will help to provide an alkalizing environment in your tissue and organs inhibiting the development and spread of cancer.

3. Support the NRF2 Pathway

It is critical to strengthen the anti-inflammatory mechanisms regulated by Nrf2 signaling in order to protect your cells against oxidative damage and free radical activity. This is why the nutrients abundant in a plant-based diet have such powerful chemopreventive properties. Phytochemicals in fruits and vegetables prevent cancer development by upregulating antioxidant enzymes and detoxification processes.

Dietary phytochemicals support the Nrf2 defenses in the following ways:

  • Inhibit the release of inflammatory promoting agents that induce metastasis
  • Protect against genetic mutations and epigenetic alterations
  • Turn off factors that keep cancer cells in a constant state of proliferation thus shutting down their ability to grow and divide
  • Shut down transcription factors responsible for turning off the body’s defense mechanisms to fight against infection

Key dietary compounds that support the Nrf2 Pathway include curcumin, resveratrol, green tea extract, and sulforaphane, among others.

Alternative Cancer Testing: Thermography

The efficacy and risks involving cancer screening is a topic globally debated. Conventional screening methods are often invasive, are a significant financial burden, increase emotional stress, expose patients to unnecessary radiation, and can even promote cancer metastasis.

An affordable and more accurate form of identifying cancer growth in the body is thermography testing. Thermography screening offers a painless and safe route for analyzing physiological changes in the body that characterize cancer growth. This diagnostic tool creates a digital map of heat patterns identifying areas where increased blood flow may indicate the presence of infection.

Unlike other diagnostic cancer screening which may only identify anatomical changes and the presence of a tumor, thermography screening provides early detection from the start of cancer growth. Any asymmetrical thermal patterns of the body provide information about abnormal vascular function helping to identify cancer before it develops the ability to metastasize.

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