Saturday, October 20, 2018

Chemotherapy and Its Side Effects: Chapter 2 - Mitotic ihibitors (Tubule inhibitors)

Chapter 2

Anticancer Drugs - C. Mitotic inhibitors (Tubule inhibitors)

Mitosis is one step of the cell cycle (Fig. 1.8) in which a cell is divided into two identical cells and each has its own nucleus. A drug that inhibits mitosis (cell division) is referred to as a mitotic inhibitor, also referred to as a tubule inhibitor. Because microtubules play a very important role in mitosis, disruption of microtubules disrupts cell division thus achieving the anticancer effect.


Tubule inhibitors, including alkaloids and terpenoids, are usually derived from plants. They usually work by interfering with microtubule function or inhibiting the assembly of microtubules; microtubules are special proteins in tubular shape that are important components of cytoskeleton, which is a dynamic skeleton in cytoplasm that maintains cell shape and plays an important role in cellular division.  Examples of this type of drug include paclitaxel and vinblastine.


Fig. 1.8   Cell cycle


© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book, "SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY", prepared by Dr. Jiajiu Shaw, Dr. Frederick Valeriote, and Dr. Ben Chen. 


Sunday, September 30, 2018

Status and Update of this Blog, September 30, 2018

Since this blog started on 9/7/2015, this blog has been viewed for 14,641 times by people around the world.

The first five countries are Israel (8,762), United States (2,796), Ireland (589), Russia (547), and Germany (546). The other viewers were from Ukraine, Brazil, United Kingdom, Japan, Spain, France, Cyprus,  Hong Kong, Canada, Italy, Thailand, Philippines, India, Malaysia, Mexico, Singapore, Chile, Argentina, Puerto Rico, Kenya, Brunel, etc. Isreal has moved up to the first place and United States of America has dropped to the second.

As to the browsers, 44% used Chrome, 29% used Firefox, 14% used Explorer, 8% used Safari, 1% used Opera, and the rest by all others. It is pretty clear that Chrome has been and is still the primary browser.

As to the operating systems, 44% used Windows, 18% used Linux, 14% used Android, 14% used Macintosh, and the rest by other systems. It is obvious that Windows is the most popular operating system.

One recent happening to share with you is that, as the principal investigator (PI), I have recently received another research grant from National Institutes of Health (NIH) of the United States to investigate a novel small molecule to reduce the side effects incurred by total body irradiation. The news release can be found on the website of 21st Century Therapeutics, www.21-cti.com.

By the way, if you’d like to read more than just my blog, you can order my second book (SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY) from amazon.com. Meanwhile, please continue to read my blog and recommend it to your loved ones and friends.


Thank you for our visit.

© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book, "SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY", prepared by Dr. Jiajiu Shaw, Dr. Frederick Valeriote, and Dr. Ben Chen. 

Saturday, September 22, 2018

Chemotherapy and Its Side Effects: Chapter 2 - Antimetabolites (Cont'd)

B.2. Fluorouracil (5-Fluorouracil or 5-FU)

Fluorouracil (Fig. 1.7) is sold under different trade names such as Adrucil and Efudex.  It is classified as an antimetabolite and has been used for treating cancer for many years. Due to its similarity to thymine, 5-FU interrupts the synthesis of thymidine, one of the building blocks of DNA. As a result, DNA replication is interrupted and the growth of cancer cells is hampered.
Fig. 1.7   5-FU (left), thymine, and thymidine (right)

Fluorouracil has been used mainly in treating colon cancer and has been used in combination with other drugs, including leucovorin, carboplatin, and paclitaxel.  It has also been used in other solid tumors including pancreatic cancer and breast cancer. Side effects of fluorouracil include myelosuppression, dermatitis, and mucositis.

© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book, "SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY", prepared by Dr. Jiajiu Shaw, Dr. Frederick Valeriote, and Dr. Ben Chen. 

Saturday, September 8, 2018

Chemotherapy and Its Side Effects: Chapter 2 - Antimetabolites (Cont'd)

B.1. Methotrexate (also referred to as amethopterin)

Methotrexate has been used for treating cancer and autoimmune diseases for many years. Although it has been off-patent for many years, it is still very highly prescribed.

Methotrexate is an antimetabolite that interferes with the use of folic acid. As shown in Figure 1.6, the structures of methotrexate and folic acid are strikingly similar. Because folic acid is essential for the synthesis and repair of DNA, especially during cell growth and division, it is logical that methotrexate interferes with the growth of cancer cells.

Methotrexate is cytotoxic and has a wide range of potential side effects including myelosuppression and mucositis. Methotrexate is also highly teratogenic and should not be taken by women during pregnancy or expected to be pregnant. It is generally true that no chemotherapy is given for pregnant women and, for women of child-bearing age, precaution must be taken.



Fig. 1.6   Structures of methotrexate (left) and folic acid (right)



Sometimes, folic acid is used to reduce the side effects of methotrexate. However, folic acid could act as an antidote to methotrexate, therefore, it is better to use folic acid on the off days during methotrexate treatment.


© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book, "SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY", prepared by Dr. Jiajiu Shaw, Dr. Frederick Valeriote, and Dr. Ben Chen. 

Saturday, August 18, 2018

Chemotherapy and Its Side Effects: Chapter 2 - Antimetabolites

Chapter 2

Anticancer Drugs - B. Antimetabolites

An antimetabolite is a drug that interferes with normal cell metabolism by inhibiting certain metabolite pathways and stopping cell growth or cell division. The molecular structure of an antimetabolite is usually similar to the metabolite that they interfere with. They usually induce cell death during the S phase of the cell cycle.

For example, folic acid is an important component in the synthesis and repair of DNA and RNA. An analog of folic acid, methotrexate, has a structure that is almost identical to that of folic acid but acts very differently; methotrexate inhibits cell division to achieve its anticancer effect.



© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book, "SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY", prepared by Dr. Jiajiu Shaw, Dr. Frederick Valeriote, and Dr. Ben Chen. 

Saturday, July 28, 2018

Chemotherapy and Its Side Effects: Chapter 2 - Alkylating Agents (Cont'd)

A.4. Cisplatin and other platinum drugs

Cisplatin, cis-dichlorodiammine platinum(II) (Fig. 1.4), is the grandparent of all platinum drugs. It is a widely prescribed anticancer drug with therapeutic activity against various solid tumors, but also with substantial side effects. The anticancer activity of cisplatin was discovered by Dr. Barnett Rosenberg of Michigan State University in 1965 [2]. In 1978, the first formulated pharmaceutical product of cisplatin, Platinol, was approved by the FDA and sold by Byistol-Myer Squibb.

As an alkylating agent, the platinum ion of cisplatin forms coordination bonds mostly with guanine on DNA. This crosslinking causes the interference of DNA replication, thus, inhibits the replication of cancer cells.

Fig. 1.4   Cisplatin, carboplatin, and oxaliplatin

Since the discovery of cisplatin’s anticancer activity, thousands of cisplatin analogues have been made and/or studied. Two of the notable platinum drugs successfully developed by Bristol-Myers Squibb are carboplatin and oxaliplatin (Fig. 1.4); both were approved by the FDA for treating a variety of cancers.

In the last thirty years or so, the impact of platinum drugs on cancer treatment has been tremendous and has benefited many cancer patients. However, because platinum drugs are often associated with significant side effects, scientists are still working on finding better platinum compounds with fewer/less side effects. Currently, there are a number of new platinum drugs under investigation or development, including some of the platinum compounds synthesized by one of the co-authors, Dr. Jiajiu Shaw. A couple of these new platinum compounds are shown in Fig. 1.5. The dinuclear platinum compound is the first to show a coordination bond between the amide oxygen and platinum(II).
Fig. 1.5  Examples of a 3-Nitrogen Pt compound (left) and a dinuclear Pt compound (right)




© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book, "SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY", prepared by Dr. Jiajiu Shaw, Dr. Frederick Valeriote, and Dr. Ben Chen. 

Saturday, July 14, 2018

Chemotherapy and Its Side Effects: Chapter 2 - Alkylating Agents (Cont'd)

A.3. Nitrosoureas


Nitrosoureas (Fig. 1.3) are another group of alkylating agents. Because of their lipid solubility, they form the basis for brain tumor treatment as they are able to cross the blood-brain barrier. Nitrosoureas can be used alone or used  in a newer technological product, Gliadel wafer


                                                                Fig. 1.3   Examples of nitrosoureas

© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book, "SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY", prepared by Dr. Jiajiu Shaw, Dr. Frederick Valeriote, and Dr. Ben Chen. 

Saturday, June 16, 2018

Chemotherapy and Its Side Effects: Chapter 2 - Alkylating Agents (Cont'd)

A.2. Cyclophosphamide

Cyclophosphamide (Fig. 1.2) is a very old anticancer drug developed in the 1950s. It is an alkylating agent that may be categorized as a nitrogen mustard.


Fig. 1.2   Cyclophosphamide and related compounds


Although cyclophosphamide (Fig. 1.2) is an analog of nitrogen mustard, it is a prodrug and inactive as opposed to nitrogen mustard. Cyclophosphamide is a prodrug (i.e., it is metabolized and become active in the body); it is metabolized in the liver by oxidase enzymes to become 4-hydroxycyclophosphamide, which co-exists with its tautomer, aldophosphamide (Fig. 1.2). 

Cyclophosphamide is administered by either i.v. injection or oral administration (25 and 50 mg tablets). It is often used in combination with other anticancer drugs to treat solid tumors in the lymphatic cells of the immune system (lymphomas) and some other types of cancers. In addition to its anticancer effect, cyclophosphamide also suppresses the immune system and is also referred to as immunosuppressive.

Potential side effects of cyclophosphamide include bone marrow suppression (causing leucopenia, anemia, and thrombocytopenia), nausea, vomiting, diarrhea, jaundice, and alopecia. Cyclophosphamide may cause kidney failure, and it also may affect the heart and lungs. Cyclophosphamide may also cause inflammation of the urinary bladder with bleeding (hemorrhagic cystitis). This can result in lower abdominal pain, problems urinating due to blood clots, and anemia due to loss of blood. 


© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book, "SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY", prepared by Dr. Jiajiu Shaw, Dr. Frederick Valeriote, and Dr. Ben Chen. 

Sunday, May 27, 2018

Chemotherapy and Its Side Effects: Chapter 2 - Alkylating Agents (Cont'd)

A.1. Nitrogen mustards

One of the first alkylating agents was nitrogen mustard, NH2 (Fig. 1.1). Nitrogen mustards are alkylating agents but are not specific in their binding site. The utility of nitrogen mustards is limited because they are very reactive and consequently very short lived.

Because of its excessive toxicity, the original nitrogen mustard, NH2, is not often used nowadays. Instead, some of its analogs or derivatives, such as cyclophosphamide, are being used.



© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book, "SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY", prepared by Dr. Jiajiu Shaw, Dr. Frederick Valeriote, and Dr. Ben Chen. 

Saturday, May 5, 2018

Chemotherapy and Its Side Effects: Chapter 2 - Alkylating Agents

Chapter 2

Anticancer Drugs - A. Alkylating Agents


A classical alkylating agent works by attaching an alkyl group or a small molecule to hinder/stop the replication of DNA in cancer cells. Classic alkylating agents include nitrogen mustard, and cyclophosphamide. Platinum drugs are a different type of alkylating agent. Instead of directly attaching an alkyl group onto DNA, a platinum drug forms coordination bonds with DNA and hampers the replication of DNA. Some examples of alkylating agents are described below.



© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book, "SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY", prepared by Dr. Jiajiu Shaw, Dr. Frederick Valeriote, and Dr. Ben Chen. 

Saturday, April 21, 2018

Chemotherapy and Its Side Effects: Chapter 2

Chapter 2
Anticancer Drugs

Chemotherapy added a major new capability to the treatment of cancer beginning with the use of alkylating agents and anti-folates in the 1940s; it continues to expand today with anticancer agents specifically targeting single subcellular structures such as proteasomes or large enzyme groups like the kinase inhibitors and anti-metabolite agents.

In addition, medical oncologists who deliver these chemical agents have become an important leg of the present therapeutic triad, which also includes surgeons and radiotherapists. This triad defines the protocol for today’s impressive treatments.

For now, let’s focus on chemotherapeutic drugs. In addition to the conventional anticancer drugs, in the last twenty years or so, many novel anticancer drugs have been developed and approved by the Food and Drug Administration (FDA).

While chemotherapy drugs may be categorized in different ways. In this book, we attempt to divide anticancer drugs into several categories according to Table 1.1 although some drugs could be placed under several categories. Another type of therapy, gene therapy, will not be discussed here.


Based on the listing in Table 1.1, a number of representative anticancer drugs will be described and discussed in the following sections.

Table 1.1.  Categories of chemotherapeutic drugs

Category
Mechanism
Example
A.      Alkylating agents
Affect DNA or cell division
nitrogen mustard, cyclophosphamide, nitrosourea,  cisplatin, oxaliplatin
B.       Antimetabolites
Affect DNA or cell division
methotrexate, 5-fluorouracil
C.      Mitotic inhibitors (Tubule inhibitors)
Affect cell division
paclitaxel, vinblastine
D.      Antibiotics (Anthrocyclines)
Affect DNA or cell division
doxorubicin, dactinomycin, bleomycin
E.       Kinase modulators

Modulate cell behaviors
imatinib
F.       Hormones

Modulate cell behaviors
tamoxifen
G.      Monoclonal antibodies
Modulate cell behaviors
cetuximab, bevacizumab
H.      Other approaches

Modulate cell behaviors
antibody + chemotherapy


© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book, "SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY", prepared by Dr. Jiajiu Shaw, Dr. Frederick Valeriote, and Dr. Ben Chen. 

Saturday, March 31, 2018

Chemotherapy and Its Side Effects: Chapter 1

Chapter 1
Introduction

     Mutation is not uncommon in our daily lives. Most mutated cells either keep their normal cellular functions or undergo a programmed cell death (apoptosis) and die at some point in time. In addition, many mutated cells are recognized and rapidly removed by the body’s immune system. Only a very small portion of mutated cells will evolve further and become cancerous cells with uncontrollable proliferation; this behavior is different from that of normal cells. For adult, most normal cells are well differentiated except for certain types of cells, such as epithelial cells and bone marrow hematopoietic progenitor cells, which are capable of continuous proliferation; unlike cancerous cells, the growth of normal cells is highly regulated and controlled.

Cancer is a group of various diseases in that some cells are mutated in certain ways so that they grow and divide continuously. Currently, there are more than 200 known cancers that afflict humans.

For the treatment of cancer, there are generally three conventional strategies: surgery, chemotherapy, and radiotherapy. In this book, we will focus on chemotherapy, radiotherapy, and their side effects.

Chemotherapy is a systemic treatment of cancer patients with one or more anticancer drugs (chemical agents) to kill cancer cells and/or slow down their growth. The name “chemotherapy” comes from chemical agents being used as a therapy for treating cancer. Chemotherapy plays a critical role in cancer treatment; it is estimated that more than half of all cancer patients receive chemotherapy.

Depending on the dosage form, cancer drugs may be administered through several different routes, including intravenous injection/infusion, oral (mouth) delivery, or a slow release dosage form embedded in a tissue by implantation. A chemotherapy regimen (a treatment plan including the dosing and schedule) usually includes the administration of at least one drug to fight cancer at a predetermined dose according to a suitable schedule, usually daily, weekly, or every several weeks. Due to the different characteristics of individual cancer drugs, the chemotherapy regimen for each drug may be different. Because cancer treatment is a delicate process, it is important to know that staying on the chemotherapy regimen gives a patient the optimal chance for a successful result.

Many times, additional supplementary drugs are used simultaneously in a chemotherapy regimen in order to achieve a better outcome to either increase the anticancer potency or reduce the side effects of chemotherapy; these drugs are often called adjuvant medications. Adjuvant drugs that are used to reduce the side effects of cancer therapy, including chemoprotective and radioprotective agents, will be discussed in Part III.

Most cancer drugs work by killing cancer cells or slowing down the growth of cancer cells. Unfortunately, most of the cancer drugs are not able to clearly distinguish between cancer cells and normal cells. Therefore, most cancer drugs will damage not only the fast-growing cancer cells but also the fast-growing normal cells, which include bone marrow cells, crypt epithelial cells (lining of small intestine), and hair follicles. In addition, a number of organs (e.g., liver, kidney, and heart) are often injured by chemotherapy.


In order to have a better understanding on how anticancer drugs work and what kind of side effects they can cause, let’s take a look at some anticancer drugs in different categories. 

© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book, "SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY", prepared by Dr. Jiajiu Shaw, Dr. Frederick Valeriote, and Dr. Ben Chen. 

Saturday, March 17, 2018

Side Effects of Chemotherapy and Radiotherapy: Preface

     Cancer is a group of diseases with similar characteristics, out-of-control growth of cancer cells. Conventional cancer treatments include surgery, chemotherapy, and radiotherapy. Although technology advancements have made vast improvements in the last two decades or so, there is no perfect treatment for cancer because of its complexity; one of the major issues related to cancer treatment is the unwanted side effects.

In the upcoming series, we will focus on the side effects induced by chemotherapy and radiotherapy. We will briefly introduce chemotherapy and radiotherapy; we will also describe the side effects, current methods to tackle the side effect issue, and how to manage the side effects.

The purpose of this coming series is to help people understand the potential side effects of chemotherapy and radiotherapy. However, it is important for you to know that this blog is not intended to substitute the expertise and judgment of your physicians or other medical practitioners.

Although the upcoming series related to side effects of chemotherapy and radiotherapy can be somewhat technical, people with some technical background in chemistry/biochemistry should be able to read through without much difficulty.

Finally, if this blog is useful for you in any way, please share it with your loved ones and friends.



Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. Most of the contents posted are extracted from the following books: (1) IS CANCER IN US, and (2) SIDE EFFECTS OF CHEMOTHERAPY AND RADIOTHERAPY. 

Sunday, March 4, 2018

Status of this blog as of March 4, 2018

As of March 4, 2018, this blog has been viewed for over 11,000 times by people around the world. The top three countries have changed a little bit. Instead of United States, Israel is now the new number one. The top ten regions are: Israel (6.683), United States (2,358), Germany (541), Russia, Ukraine, Brazil, Taiwan, Hong Kong, China, and France. Many people in other regions in the world also viewed this blog. Thank you for viewing my blog and I sincerely hope that you can learn something here.

In the near future, we will talk about a somewhat different topic: side effects of chemotherapy and radiotherapy. With the help from Dr. Frederick and Dr. Ben Chen, we published a book on this important subject, which is available at amazon. In the upcoming blogs, I will share with you most of the important contents of this book.

Furthermore, I plant to share with you my experience in fighting against my pancreatic tumor. My complete experience has been published as my 3rd book, HOW I FOUGHT AGAINST MY PANCREATIC TUMOR, published in March of 2017. If you don't have the book, you can look forward to seeing most of the contents here in this blog. Please be patient as I am just beginning to cover another important topic: Side Effects of Chemotherapy and Radiotherapy.

If you like what you read, please continue to read my blog and recommend it to your loved ones and friends. Thank you for your visiting.
  

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. 

Saturday, February 10, 2018

Additional Information and Other Common Questions (3)

Regular Testing and Early Detection

The second important strategy to fight against cancer is to do regular testing.  If anything on your body appears suspicious, it is much easier to deal with it in the early stage.  If you remember the analogy of taking care of the lawn, dealing with just a few dandelions in the early stage is much easier than dealing with a whole bunch of dandelions in the later stage.  This strategy works similarly in cancer treatment; early detection is the best way to start dealing with cancer.

Self-Examination

Self-awareness and self-examination are very important in cancer screening.  Let’s briefly use skin cancer as an example.  Skin cancers found and removed early are almost always curable.  Self-examination of the skin is not too difficult to perform except the back for that you may need someone else to help.  Basically, one should look carefully for any new or changing lesions that might be cancerous or precancerous. If you spot anything suspicious, see a doctor.  Self-examination should be done regularly; it is a small investment but it could be life-saving.

For other cancer such as breast cancer and testicular cancer, self-examination can also be very important.  Because different types of cancer require different techniques in self-examination, we won’t go into too many details.  It is suggested that you look up the self-examination procedure for individual cancers from other resources and consult with your physician. 

Cancer Screening by Professionals

As mentioned, early detection is a very important step in fighting against cancer.  If any cancer is detected early, it is much easier to treat.  I have several relatives diagnosed with cancer early enough and they are all doing well for over five years.

Indeed, cancer screening by medical professionals is very important.  However, one needs to keep in mind that some tests might create certain potential issues.  For example, some tests might give false-positive results, wherein the results indicate that cancer may be present but it is in fact not present.  Also, some test might show the false-negative results indicating cancer is not there although cancer is present.  Therefore, it is a good idea to have the screening done by a different method or by a second lab in order to be absolutely sure.  Sometimes, it may be necessary to do a biopsy for cancer screening.

New Cancer Diagnosis

One of the new methods in cancer diagnosis is the use of liquid biopsy.  Liquid biopsy is different from traditional biopsy wherein a tiny piece of living tissues is removed for diagnostic testing. Basically, in liquid biopsy, a small quantity of body fluid (blood, urine, etc.), instead of a tissue part, is taken for cancer diagnosis. 

Nowadays, the term, liquid biopsy, is becoming more popular in the field of cancer diagnosis and management.  Modern biotechnologies make it easier to detect more biomarkers more sensitively.    

For cancer liquid biopsies, the analyses are basically done on three categories: circulating tumor cells (CTCs), circulating tumor DNA (ctDNA), and exosomes.  Detection of CTCs was first thought to be a useful tool many years ago but never became practical. In recent years, due to advanced biotechnologies, the analysis of ctDNA or exosomes is becoming more practical. Liquid biopsies make it easier for gene profiling and to identify which mutations are driving the growth of cancer. At the present time, some companies are already offering liquid biopsy tests for gene alterations to help cancer treatment.

What are the advantages of liquid biopsy as compared to conventional biopsy? For a conventional biopsy, a small piece of potential tumor tissue is taken; it could be painful and might not be a true representation of the molecular profile. On the other hand, liquid biopsy is non-invasive and less painful.  In addition, it could detect the heterogeneity of cancer. Therefore, it is easier to take a series of samples so that the tumor genomic can be monitored in a time course and easier to make adjustment in cancer treatment. Furthermore, liquid biopsies can be used as a potential screen for cancer.

Although liquid biopsy does not completely replace regular biopsy, it can be very useful in some cases, particularly in cancer diagnostics. For example, when a tumor is located at some site that is not easily accessible, regular biopsy could require more work and the patient may suffer significant pain.  In terms of early detection, liquid biopsy may be used to identify ctDNA to detect potential tumor that is not known or identified by other methods.


© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book I wrote, "IS CANCER IN US", published recently.

Saturday, January 27, 2018

Additional Information and Other Common Questions (2)

Can we do something about the “bad luck”

Let’s ask ourselves, even though we have no choice for the trip provided to us (the journey of our lives provided by nature), there is a lot we can do to make the trips safer and with fewer chances of getting involved with accidents.  For example, we can make sure the car is well maintained and we can drive more carefully by not speeding and not tailgating.  I believe that this strategy works similarly in reducing the risk of cancer. 

We can reduce bad foods and eat healthful foods; we can do regular exercise instead of being lazy; we can relax as needed instead of being under stress all the time; we can get rid of our bad habits (e.g., smoking and heavy drinking); we can avoid exposure to carcinogens and bad living environment.  All these could make the journeys of our normal/stem cells (i.e., cell cycles) safer and with fewer accidents, i.e., lower the chances for cell mutation to become cancerous. 

In addition, by doing the right things onto ourselves (eventually onto our normal/stem cells), we can maintain healthier cell cycles for our normal/stem cells so that the check points in the cycles (G1, G2, M check points) are less prone to mistakes.  If the check points are not healthy, they tend to allow damaged cells to continue the cell cycle to grow or divide and they might become cancer cells.  The other aspect about stem cells is the duration of cell cycle.  Some stem cells in the body don’t reproduce as quickly as the others; some stem cells may be stimulated by the environmental factors to grow and reproduce faster.  In this case, some things can be done to reduce the stimulation and then slow down the growth/replication of stem cells.  Therefore, it is possible to take some actions to reduce the chances of bad luck from happening.

In short, don’t be discouraged by the two-thirds of bad luck; many of them are attributable to macro- and micro-environmental factors, on which we do have some control.

Yes, accidents do happen in many aspects of one’s life.  Theoretically, anyone may be subject to the possibility of an accident such as earthquake, tornado, flood, robbery, car accident, etc.  However, one can always reduce the chances for the accidents to happen.  For example, one does not have to live in an earthquake zone; one can also live in an area with lower frequency of tornados, a higher area with lower flood opportunities, and areas with lower crime rates.  By doing so, can anyone say that he or she is 100% free from of any accident?  The answer is NO.  That’s why we need life insurance, home insurance, and auto insurance.  However, the chances of accidents happening can be significantly reduced by one’s proactive actions. 

I think you’ll agree that there is no guarantee for anything.  Unfortunately, that is how life is.  For cancer prevention, all we can do is to reduce the chance of getting it.  With today’s knowledge derived from the research work by thousands of scientists, we can really significantly reduce the chances of getting cancer.


In summary, although no one can guarantee that he or she will never get cancer, but there is a lot one can do to significantly reduce the chances of getting cancer. 

© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book I wrote, "IS CANCER IN US", published recently.

Saturday, January 6, 2018

Additional Information and Other Common Questions (1)

Cancer and bad luck

Most people would agree that prevention is the best strategy to reduce the chances of getting cancer; there have been numerous reports and books talking about cancer prevention.  However, there are also a wide range of new reports about cancer coming out from time to time.

Recently, Dr. Cristian Tomasetti and Dr. Bert Vogelstein from the Johns Hopkins Kimmel Cancer Center used a statistical model to measure the proportion of cancer risk across many tissue types.  “All cancers are caused by a combination of bad luck, the environment and heredity, and we’ve created a model that may help quantify how much of these three factors contribute to cancer development,” according to Dr. Vogelstein.  Based on their studies, two-thirds of the variation in adult cancer risk can be explained primarily by bad luck, when specific mutations occur while stem cells divided, and the remaining one-third are due to environmental factors and inherited genes.

If we look only on the surface of the report, it is easy to get discouraged by their finding.  According to the website of Johns Hopkins regarding their research work, “Getting cancer could be compared to getting into a car accident.  Our results would be equivalent to showing a high correlation between length of trip and getting into an accident. Every accident is caused by some combination of road conditions, car conditions, length of the trip and other factors”.


Therefore, some people may be misled to think that two-thirds of cancer risks are simply by bad luck and don’t do anything to prevent cancer.  However, if we were to look deeper into their conclusion and do a little more pondering, we could see some positive side of the report. 

© Jiajiu Shaw, 2018

Disclaimer: This blog is written solely for informational purposes. It does not constitute the practice of any medical, nursing or other medical professional health care advice, diagnosis, or treatment. All contents posted are extracted from the book I wrote, "IS CANCER IN US", published recently.