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Why people get cancer, how it spreads and how to prevent it

Solving a Pandemic

By Tafara SibotshiwePublished 12 months ago 5 min read
Why people get cancer, how it spreads and how to prevent it
Photo by National Cancer Institute on Unsplash

Consider that our body functions like a community. It consists of more than 30 to 40 trillion cells that work together symbiotically. We have a digestive system that processes food, acting as a food and cleaning machinery. Additionally, our body has various systems, including an immune response, which serves as an army to protect against foreign invaders. This symbiosis is crucial for maintaining health, not only in the animal kingdom but also in our human body.

Unfortunately, cancer remains a significant issue. It does not discriminate against age, gender, ethnicity, or wealth. It invades our lives and affects our health, happiness, and financial well-being. Thus, it is essential to understand the nature of cancer, including its causes and how we can prevent it.

According to data from 2020, nearly 20 million people worldwide were diagnosed with cancer, resulting in about 10 million deaths. In the United States, however, there is good news: the incidence of cancer has been declining each year. Data shows a downward trend in cancer incidence for both men and women, as well as a reduction in cancer-related mortality. Over the last decade, advancements in diagnostics and treatment options have saved approximately 2.5 million men and 1.5 million women.

Despite these advances, pancreatic cancer poses a significant challenge, as both its incidence and mortality rates are increasing for both genders. It is crucial to deepen our understanding of this type of cancer.

When it comes to cancer treatment, early detection is vital. For example, the survival rate for localized breast cancer is around 99%. However, if the cancer has metastasized to other organs, like the liver or pancreas, the survival rate dramatically decreases.

Let us examine three major types of cancer: sporadic, hereditary, and familial. Sporadic cancer typically arises from lifestyle choices. Hereditary cancer is caused by mutations passed from parents to offspring. Familial cancer represents a combination of hereditary factors and environmental influences.

Understanding cancer at a cellular level is fundamental. Each cell contains chromosomes, which are made up of DNA. DNA produces genes. To explain, think of DNA as the roadways in a city, while genes are specific streets. Each cell houses a meter-long strand of DNA, with small segments that are considered genes.

Cancer occurs when specific mutations affect cellular mechanisms. Consider each cell as a car on a road. Cars have brakes and accelerators. If a cell develops a mutation in its tumor suppressor genes, it is akin to losing the brakes, while a mutation in oncogenes is like pressing the accelerator more than necessary. With functioning brakes and a full gas tank, a car can be controlled; similarly, cells require regulation to prevent uncontrolled growth.

A critical player in this process is telemorase, an enzyme that adds telomeres to chromosomes. In healthy cells, this enzyme has a limited function to ensure that cells eventually stop dividing and die through a process known as programmed cell death. In cancerous cells, however, telomerase is activated indefinitely, allowing continuous division.

Cancer is primarily an age-associated disease. As we age, we accumulate mutations through lifestyle, leading to a higher likelihood of developing cancer later in life. Notably, inheriting a mutation does not guarantee cancer development. A person may inherit a mutation and still remain cancer-free, as multiple steps must be completed before a normal cell becomes cancerous.

Environmental factors such as pollution, alcohol intake, and stress significantly influence cancer susceptibility. Maintaining a healthy lifestyle can help mitigate risks. Furthermore, our microbiome, composed of approximately 38 trillion bacteria, is vital for our health, and we must respect its balance.

Research has shown that it is possible to convert a normal cell into a cancerous one in a laboratory by inactivating tumor suppressor genes and activating oncogenes. The resulting cancer cells can metastasize if they overcome certain barriers and transition from tightly adhered epithelial cells to more mobile mesenchymal cells.

As a pathologist studies tumors, they can often determine the primary source of a tumor based on structural similarities to other types of tissue. It has been hypothesized that tumor cells can behave like stem cells, leading to metastasis and treatment resistance. Consequently, targeting cancer stem cells is a vital area of research.

Historically, cancer treatment has focused on single modalities, such as chemotherapy. However, precision oncology now allows for individualized treatment based on specific genetic mutations within a patient's tumor. Using targeted therapies can enhance treatment efficacy and minimize side effects.

Ongoing forward leaps in disease treatment are remarkable. For instance, Jim Allison has made critical headways in disease treatment. He found that growth cells can fool insusceptible cells into saving them. These growth cells convey a message that makes the resistant cells think they are companions. By impeding this sign, Allison empowers resistant cells to assault and kill cancer cells. This advancement has changed the viewpoint for patients with melanoma. Recently viewed as a capital punishment, melanoma can now be dealt with successfully with immunotherapy.

Advancements in malignant growth screening are additionally significant. For example, customary colonoscopies for malignant growth recognition were frequently hard for patients. Today, an organization has made a little camera that can be ingested like a pill. This camera goes through the stomach related framework and catches pictures of the whole stomach. Moreover, Olive Diagnostics has fostered a latrine seat that dissects pee for any irregularities while being used, giving important wellbeing data.

Another interesting idea is Computerized Twins. As people ceaselessly give information through wearables and genomic sequencing, organizations can make advanced imitations of patients. These computerized twins can assist with anticipating the drugs required for every individual. A striking model is the send off of Gemini, a computerized twin undertaking pointed toward treating numerous myeloma.

The expense of genome sequencing has definitely diminished. At first, sequencing a genome cost around $100 million. Presently, it very well may be finished for just $500 to $800. This decrease considers more far reaching sequencing, taking care of the data into supercomputers. The objective is to speed up custom-made therapy choices for malignant growth patients.

Before, different specialists like pathologists, clinicians, oncologists, and essential researchers worked to some degree cooperatively however not as a strong group. At the Legorreta Malignant growth Place and across the globe, experts are presently shaping groups. This cooperative methodology plans to target and battle malignant growth really.

The group at Earthy colored College and the Legorreta Malignant growth Community is committed to this mission. The fate of disease treatment is promising. Early finding fundamentally increments endurance rates. It is pivotal to advocate for malignant growth research, partake in clinical preliminaries, and bring issues to light. Early location can prompt treatable results. In this manner, looking for ideal and precise diagnosis is fundamental.

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About the Creator

Tafara Sibotshiwe

A versatile authentic writer and passionate storyteller. With a background in, Journalism, Engineering, History, Health & finance, they combine profound insight with creative flair to explore the complexities of the human experience.

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