PANCREATIC CANCER: DISCOVERY OF FIRST STEPS FOR ITS OCCURRENCE.

PANCREATIC CANCER: DISCOVERY OF FIRST STEPS FOR ITS OCCURRENCE.

(© 11 November, 2014: Dr. V.M. Palaniappan, Ph.D.)

I read with great interest today’s Science X Newsletter Monday, Nov 10: under Medicine & Health News an interesting article about the discovery of a first step for the recognition PANCREATIC CANCER.

In this regard, you may want to read the original article, by clicking the URL: https://mail.google.com/mail/u/0/?tab=wm#inbox/1499cb5f967cecfa

Anyway, the original article comes from CANCER DISCOVERY journal. That is published by the American Association for Cancer Research, whose website is: http://cancerdiscovery.aacrjournals.org/ If you wish, you can reach that through: http://medicalxpress.com/journals/cancer-discovery/

OR,through:

http://medicalxpress.com/news/2014-11-formation-pancreatic-cancer.html?utm_source=nwletter&utm_ medium email &utm_ content=ctgr-item&utm_campaign=daily-nwletter
Mayo Clinic   You can reach Mayo clinic’s URL too.

It says: 

Researchers identify first steps in formation of pancreatic cancer

Researchers at Mayo Clinic's campus in Jacksonville say they have identified first steps in the origin of pancreatic cancer and that their findings suggest preventive strategies to explore.

They have described that the digestive enzyme releasing enzymes, called the ACINAR cells present in the Pancreas, become PANCREATIC LESIONS. Some of these can turn into cancer.

Pancreatic cancer is said to develop from these lesions.

The Lead Scientist, a Biologist like me, Dr. Peter Storz, Ph.D. says that if we can understand HOW THESE LESIONS COME ABOUT, WE MAY BE ABLE STOP THE CANCER ALTOGETHER.

According to him, the need for new treatment and prevention strategies is pressing. He has noted that the cancer symptoms do not occur until the cancer is well advanced.

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Well, Dear Readers,

I have the following suggestion, based on MY OWN RESEARCH / FINDINGS, and THIS information should help Dr. Peter Storz in his attempt to stop the cancer altogether.  

KINDLY NOTE: I HAVE ALREADY SUCCEEDED IN STOPPING IT.  Let me share some of the relevant information I know in this regard.

Whether you like it or not, FOR THE TIME BEING, please accept my finding that ALL cancers are the results of EXCESSIVE CALCIUM.

(If you find my explanation a non-sense, you can then dismiss the idea LATER.)

In humans, being day-time ‘animals’, based on Circadian Rhythm, ingested food will get digested during day-time.

If a person consumes food late-night, say by 10 p.m. or so, the ingested food does NOT get digested until next morning.

Not only that, the food, which are in the form of bolus, get stagnated here and there along the intestinal tract, for the PERISTALSIS ACTION declines as night falls, and stops totally after 10.00 p.m. or so - until about the time of sunrise next morning.

The stagnated food tends to release all the water soluble nutrients that do not require any digestive enzyme.

Calcium mineral, being highly water-soluble, gets absorbed by the inner wall of the intestine – by the glandular adenomatous cells that line the ‘lumen’ of the intestinal tract.

These cells, because of imbibing TOO much of calcium, tend to swell up.

A continuous inflow of calcium would continuously increase cellular contents and would pressurize the cell walls.

For want of choice, each of these swollen cells splits into two, thus resulting in asexual mitotic cell division.

As a result of continued cell divisions of this kind, the entire structure swells up, looking like inflammation. 

This process tends to occur in all pancreatic cancers. 

This happens because, there is no other structure that can share the imbibed extra free calcium absorbed from the stagnated food bolus from the duodenum part of the intestine.

Therefore, I think, it may not be correct to designate the above process as a KRAS genetic mutation, as has been suggested by the lead researcher Dr. Peter Storz.

Kras could be producing a protein that regulated the cell division. 

However, it may not be correct to suggest that it is a genetic mutation. In my opinion, it is sheer pressure exertion on the walls from the increased volume of the cytoplasm due to simple absorption of the free calcium excesses, in greater abundance, beyond the tolerance capacity of the cell itself.

The cells, instead of rupturing, divide mitotically to accommodate the oncoming calcium excesses.

Naturally, when a large number of cells have formed due to continued mitotic cell divisions that are necessitated by the continued flow of excessive calcium (through late-night dinings, night after night, for a prolonged period), they are bound to form a structure, similar to a LUMP (in the breast).

Dr. Peter Storz has recognized that the Kras proteins in the Acinar cells give rise to ICAM-1, and that attracts certain IMMUNE CELLS.

Different types of cells of that kind form the the PRECANCEROUS PANCREATIC LESIONS.

According to him, prevention of the above process should be able to prevent the pancreatic cancer formation.

He is correct.

As per my finding, the following understanding and sequence would achieve it:

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I have explained in my previous publications that it is the presence of CALCIUM WITHIN THE BODY THAT PRODUCES IMMUNITY (Palaniappan, 1998).

 IN OTHER WORDS, IF A PERSON’S BODY LACKS ADEQUATE CALCIUM, OR IF SEVERE CALCIUM DEPLETION OCCURS, THEN, THE PERSON LOSES HIS IMMUNITY AGAINST VIRUS DISEASES.

Blood tests show the presence of immunity, if the person’s body has accumulated calcium.

Often,a person whose body does not have excesses of free calcium, the blood tests show that the person does NOT have immunity.

In other words, it is excessive CALCIUM that  provide the IMMUNITY against VIRUS diseases*.

(* Virus lives in acid medium Alkaline medium prevents the very existence of viruses. I have established this in several of my publications.

In fact, the cure for chickenpox caused by virus is to bathe the body of an infected person with water that is alkalized by lime - calcium.)

According to Dr. Peter Storz, "Understanding the crosstalk between acinar cells with Kras mutations and the microenvironment of those cells is key to developing targeted strategies to prevent and treat this cancer," he says.

This appears to be correct.

THIS CAN BE ACHIEVED BY SIMPLY DE-CALCIFYING THE PERSON’S BODY THROUGH SIMPLE METHODS I HAVE ALREADY ESTABLISHED.

The procedure dictates that:

(a)  the person should drink about 2 L (or more) of water daily. Distilled or rain water, being edible and acidic, speeds up the process of calcium depletion; 

(b) void nearly all of the consumed water as urine, through about 9 urinations daily,

(c) ascertaining that the faeces moves out in good shape, and is not slimy*, lest, it would release the unutilized calcium component present in the undigested faecal matter, thus giving rise to morbid obesity, followed by colon cancer, and

(* Faeces would turn slimy if a person consumes chocolates, biscuits, peanuts, over-ripe fruits, especially papaya, excessive fibre-containing synthetics, and the like.)

(d)  all calcium-enriched eatables and supplements should be totally avoided. Also, avoidance of naturally-calcium rich food items such as sea food (crabs, prawns, anchovies, fish, etc.) WOULD HELP TREMENDOUSLY IN THE PREVENTION, AS WELL AS THE CURATIVE PROCEDURE OF PANCREATIC CANCER.

On doing the above, which takes about three weeks, the Pancreatic Lesions can be reversed easily.

As for curing the Pancreatic Cancer, the patient may have to take edible acid herbs or their extracts to gradually dissolve the accumulated calcium excesses, and to eliminate such excesses from the body altogether, leaving only the ‘WANTED’ or required calcium behind.

I have described clear-cut procedures for the above in several of my publications, including Obesity: Causes Cure and Prevention (1998), and Cancer: Causes, Cure and Prevention. (2010).

My book "The True Causes of All Diseases" has excellent information related to the calcium dynamics in relation of major diseases that affect humans.

I will be happy to coordinate if the internationally-famous Mayo Clinic invites me to be in the research time, together with Dr. Peter Storz, provided that they give me due recognition, not as a subordinate lab-assistant, but as a Prime Investigator, on par with him.

Will they do it, for the sake of human welfare?

With best wishes, and thanks for reading this,

Dr. Palani, Ph.D.