
IISc researchers develop new imaging method to detect tumours
The molecule, called GPc, is created by scientists from the Department of Bioengineering at IISc and designed for use with Photoacoustic (PA) Tomography, a relatively new imaging technique. Their work could open the door to safer and more affordable tumour detection, especially for tumours located close to the body's surface.
Tumour cells are far more active than healthy ones and consume a lot more glucose. PET (Positron Emission Tomography) scans — currently the gold standard in cancer imaging — take advantage of this by injecting patients with a radioactive sugar molecule called 18F-FDG. This sugar builds up in tumours, helping doctors spot them. But PET scans are expensive and repeated scans can expose patients to harmful radiation over time.
Photoacoustic Tomography uses a safer approach. A near-infrared laser beam is directed at special light-absorbing molecules, called chromophores, which slightly expand and create tiny pressure waves when heated. These waves can be detected as sound signals and processed into 3D images. The method is less costly than PET or MRI and works well for mapping superficial tumours.
At present, clinical PA imaging mostly relies on natural chromophores already found in the body, such as haemoglobin. But haemoglobin's signals, while useful, are not strong enough for certain diagnostic needs. This is where IISc's innovation comes in.
The team conducted several experiments to see whether GPc enters cells the same way glucose does and whether it competes with glucose for entry. This was important because if GPc behaved like a glucose 'agonist', entering cells and being metabolised, it might not work as a good imaging agent. The results were promising. GPc entered tumour cells easily, was not metabolised, and did not depend on GLUT1 transporters (the proteins that normally carry glucose into cells).
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


The Hindu
2 hours ago
- The Hindu
IISc study highlights how H5N1 influenza poses serious risk to humans
The H5N1 influenza virus, which was first identified in birds three decades ago, has now gradually found its way to humans. Indian Institute of Science (IISc) researchers in a new study have discovered that the currently circulating 2.3.4.4b clade of H5N1 has specific mutations in its genome that increase its human adaptive potential. H5N1 is a strain of the influenza virus harbouring type 5 haemagglutinin (H5) and type 1 neuraminidase (N1) surface proteins, which help in viral entry and spread, respectively. Common ancestor IISc said that clade represents a group of organisms having a common ancestor. 'The 2.3.4.4b clade has infected many mammalian species and is adapting to [non-human] mammals, which is a concern for human adaptation. The clade is panzootic, causing unprecedented mortality in birds and mammals, along with several sporadic human infections,' Kesavardhana Sannula, assistant professor in the Department of Biochemistry, IISc. Growing risk According to Ranjana Nataraj, project associate at the Department of Biochemistry and the study's first author, this clade is acquiring the same key mutations that pandemic human influenza strains possess, which could be a growing risk. IISc said that when the influenza virus enters a new organism, it can develop genetic mutations. This helps the virus adapt to the new host. The researchers were trying to decode whether the 2.3.4.4b clade was evolving to produce crucial adaptations in its proteins that allow it to infect humans. They also wanted to decipher which host animals can potentially accelerate this adaptation, giving the virus a leg up in scaling the evolutionary ladder. Mr. Sannula's team took a computational approach and analysed 7,000 protein sequences of 2.3.4.4b H5N1 found in birds, 820 sequences from non-human mammals, and 35,000 human H1N1 and H3N2 sequences, in order to identify which amino acids are under selection pressure – rapidly changing. They used multiple sequence alignment (a tool to identify similar regions in multiple proteins), constructed phylogenetic trees (which represent how species have diverged from their common ancestor over time), and annotated specific variations in all the proteins of H5N1 infecting non-human mammals and humans. Increased mutations The team found an increased number of mutations specifically in the viral polymerase complex (PA, PB2), nucleoproteins, and haemagglutinin (HA) proteins. IISc said that once it identified these mutations, the team classified them depending on whether the mutations can help the virus spread from non-human mammals to humans (adaptive) or simply survive in the non-human host (barrier). 'Finally, they developed a simple mathematical approach and estimated the human adaptive potential for the 2.3.4.4b clade,' IISc said. The team was also able to pinpoint animals that would be likely to harbour virus strains with the highest human adaptive potential. Interestingly, viruses that can adapt to fox hosts seemed to have higher adaptive potential than cattle-adapted strains. Based on their findings, the researchers suggest that enhanced and proactive surveillance measures need to be implemented.


Time of India
6 hours ago
- Time of India
IISc study warns of rising human infection risk from evolving bird flu strain
Infographic depicting key finding | Credit: IISc BENGALURU: Three decades after the H5N1 influenza virus was first detected in birds, scientists say a particular branch of the virus is inching closer to becoming a serious human threat. Researchers at the Indian Institute of Science (IISc) in Bengaluru have identified specific genetic mutations in the currently circulating 2.3.4.4b clade that may be increasing its potential to infect people. 'This clade has infected many mammalian species and is adapting to [non-human] mammals, which is a concern for human adaptation…It is panzootic, causing unprecedented mortality in birds and mammals, along with several sporadic human infections,' Kesavardhana Sannula, assistant professor in IISc's Department of Biochemistry, who led the study, said. H5N1's surface proteins — type 5 haemagglutinin (H5) for cell entry and type 1 neuraminidase (N1) for viral spread — are key to its infectivity. When the virus jumps to a new host, mutations in its genome can help it survive, and sometimes thrive, in the new environment. The IISc team set out to examine whether the 2.3.4.4b clade was evolving proteins that could make the leap to humans easier — and which animal hosts might be accelerating that shift, IISc said Tuesday. Using computational tools, the team analysed nearly 43,000 protein sequences: 7,000 from birds, 820 from non-human mammals, and 35,000 from human influenza strains H1N1 and H3N2. They looked for amino acids under 'selection pressure'— rapidly changing regions — and tracked how these mutations were distributed across the viral polymerase complex, nucleoproteins, and haemagglutinin. by Taboola by Taboola Sponsored Links Sponsored Links Promoted Links Promoted Links You May Like Calcutta Users Prefers Toothsi Aligners Toothsi by MakeO Book Now Undo The mutations were then sorted into two categories: adaptive (helping the virus infect humans) and barrier (hindering cross-species spread). Their model also ranked potential animal hosts by the risk their adapted viruses could pose to humans. Fox-adapted strains, surprisingly, appeared more dangerous than cattle-adapted ones. 'This clade is acquiring the same key mutations that pandemic human influenza strains possess, which could be a growing risk,' said Ranjana Nataraj, the study's first author. The findings, the researchers argue, make a strong case for proactive, targeted surveillance — especially in mammals that can act as 'stepping stone' hosts for the virus's adaptation to humans.


Time of India
7 hours ago
- Time of India
IISc, startup develop magnetic nanobots to treat tooth sensitivity
BENGALURU: For millions of people, the sudden, sharp pain of tooth sensitivity can turn a sip of cold water into a jolt. Now, researchers at the Indian Institute of Science ( IISc ), in collaboration with Bengaluru-based deep-tech startup Theranautilus, have engineered 'CalBots' – magnetic nanobots that can seal the problem at its source. As per IISc, CalBots are 400-nanometre particles loaded with a calcium silicate-based bioceramic formula, designed to travel deep inside dentinal tubules, the tiny tunnels in the tooth that lead to nerve endings. Guided by an external magnetic field, the bots can penetrate up to 500 micrometres into the tubules and self-assemble into stable, cement-like plugs that recreate the tooth's natural barrier. One application, the team says, can offer lasting relief. Dental hypersensitivity affects nearly one in four people worldwide and occurs when enamel erosion or gum recession exposes the dentine layer beneath, IISc said. The tubules in dentine act as direct pathways to the nerves, which is why even mild temperature changes can trigger pain. by Taboola by Taboola Sponsored Links Sponsored Links Promoted Links Promoted Links You May Like The Most Beautiful Female Athletes Right Now Undo 'We didn't want to create a slightly better version of what's already out there. We wanted a technology that solves a real problem in a way that no one's attempted before,' Shanmukh Peddi, postdoctoral researcher at IISc's Centre for Nano Science and Engineering (CeNSE) and co-founder of Theranautilus. The team used a completely new class of bioceramic cement for the nanobots. While bioceramics are common in orthopaedics and dentistry, the formulation was designed specifically for hypersensitivity – to travel deeper and last longer. To test the approach, they worked first on extracted human teeth. 'On these samples, we applied CalBots under a magnetic field for 20 minutes, during which the bots sealed the dentinal tubules by forming deep, stable plugs – a result confirmed through high-resolution imaging,' Peddi said. They then moved to animal trials, inducing sensitivity in mice and tracking their drinking behaviour. 'Healthy mice drank both cold and room temperature water equally. But sensitive mice completely avoided cold water. After treatment, they started drinking it again. We saw 100% behavioural recovery. That was a big moment for us,' he said. The CalBots are made entirely from materials classified as 'Generally Recognised as Safe' and passed toxicity tests in mice. 'This is a compelling demonstration of what nanorobotics can achieve, and how they could significantly impact future healthcare,' said Ambarish Ghosh, professor at CeNSE and one of the study's corresponding authors. Debayan Dasgupta, former PhD student at CeNSE and co-founder of Theranautilus, sees this as part of a bigger technological shift. 'We've created a regenerative, active nanomaterial – a step towards the kind of 'tiny mechanical surgeons' Richard Feynman once envisioned,' he said. Peddi added: 'This is something we've worked towards silently for years. And the fact that we've done it here, in India, makes us very happy.'