Bangladeshi scientist, two researchers make cancer test as simple as blood test


FE Team | Published: December 09, 2018 12:10:30 | Updated: December 12, 2018 13:55:56


Bangladeshi scientist Abu Ali Ibn Sina. Photo courtesy of Sabiha Sultana via Facebook

A Bangladeshi scientist and two other researchers have made a breakthrough in cancer testing by inventing a new method that is as simple as a blood test.

But it will still take time to make the test commercially available as clinical trials are needed before they know for sure if it can be used in the hospitals.

The researchers of the University of Queensland wrote the details of their research on the World Economic Forum website after it was published in the journal ‘Nature Communications’ on Dec 4.

Forbes magazine has also published the story of the test that could be used to diagnose all types of cancer.

Abu Ali Ibn Sina, who was a teacher at the Shahjalal University of Science and Technology in Sylhet, works as a research fellow at the University of Queensland under Prof Matt Trau. Another researcher was Laura Carrascosa, a postdoctoral research fellow.

What is it?

It is based on a unique DNA signature that appears to be common across cancer types, the researchers wrote on the World Economic Forum website.

Each cancer type, be it breast or bowel cancer, has different genetic and other features. Usually a test that detects one cancer may not work on another.

Researchers have long been looking for a commonality among the variants of cancer to develop a diagnostic tool that could apply across all types.

“Our research has found that cancer DNA forms a unique structure when placed in water. The structure is the same in DNA from samples of breast, prostate and bowel cancers, as well as lymphoma.

“We used this discovery to develop a test that can identify the cancerous DNA in less than ten minutes,” they wrote.

This is what the researchers wrote in the World Economic Forum --

Current detection of cancer requires a tissue biopsy – a surgical procedure to collect tissue from the patient’s tumour.

Researchers have been looking for a less invasive diagnostic test that can detect cancers at an earlier stage.

Nearly every cell in a person’s body has the same DNA, but studies have found that cancer’s progression causes this DNA to undergo considerable reprogramming.

This change is particularly evident in the distribution pattern of a tiny molecule called a methyl group, which decorates the DNA.

A normal cell DNA’s distinct methyl pattern is crucial to regulating its machinery and maintaining its functions.

It is also responsible for turning genes on and off. Altering this pattern is one of the ways cancer cells regulate their own proliferation.

This methyl patterning has been studied before.

However, its effect in a solution (such as water) has never been explored.

Using transmission electron microscopy (a high-resolution microscope), we saw that cancerous DNA fragments folded into three-dimensional structures in water.

These were different to what we saw with normal tissue DNA in the water.

In the lab, gold particles are commonly used to help detect biological molecules (such as DNA).

This is because gold can affect molecular behaviour in a way that causes visible colour changes.

We discovered that cancerous DNA has a strong affinity towards gold, which means it strongly binds to the gold particles.

This finding directed us to develop a test that can detect cancerous DNA in blood and tissue.

This requires a tiny amount of purified DNA to be mixed with some drops of gold particle solution.

By simply observing the colour change, it is possible to identify the cancerous DNA with the naked eye within five minutes.

The test also works for electrochemical detection – when the DNA is attached onto flat gold electrodes.

Since cancer DNA has higher affinity to gold, it provides a higher relative electrochemical current signal in comparison to normal DNA.

This electrochemical method is highly sensitive and could also eventually be used as a diagnostic tool.

Why this matters

For this test to work properly the DNA must be pure.

“So far we have tested more than 200 tissue and blood samples, with 90 per cent accuracy,” they said.

“Accuracy is important to ensure there are fewer false positives – wrongly detecting cancer when there is none.

“The types of cancers we tested included breast, prostate, bowel and lymphoma. We have not yet tested other cancers, but because the methylation pattern is similar across all cancers it is likely the DNA will respond in the same way.”

It is a promising start, though further analysis with more samples is needed to prove its clinical use.

The next step is to do a large clinical study to understand how early a cancer can be detected based on this novel DNA signature, reports bdnews24.

“We are assessing the possibility to detect different cancer types from different body fluids from early to later stages of cancer,” they wrote.

“We are also considering whether the test could help monitor treatment responses based on the abundance of DNA signatures in body fluid during treatment,” the researchers added.

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