Health
Oxidative Stress Linked to Development of Cancer, Cardiovascular Diseases: Study
This breakthrough could pave the way for new therapeutic approaches targeting oxidative stress, offering hope for the treatment of a wide range of diseases where antioxidant responses are vital.

A new study by researchers at the Rajiv Gandhi Centre for Biotechnology (RGCB), Kerala, India, has revealed a crucial connection between mRNA processing and oxidative stress response, shedding light on a condition that plays a pivotal role in the development of various diseases, including cancer, cardiovascular disorders, neurological diseases, and diabetes, as well as aging. The research emphasizes the critical impact of oxidative stress, particularly in the heart, which contributes to several health conditions such as hypertension, heart failure, hypoxia, ischemia-reperfusion injury, atherosclerosis, and hypertrophy (excessive development of an organ or tissue).
The team of scientists at RGCB, led by Dr. Rakesh S. Laishram (Scientist), Dr. Feba Shaji, and Dr. Jamshaid Ali, discovered that during oxidative stress, when reactive oxidative species exceed the cell’s capacity to neutralize them, the production of antioxidant proteins is boosted. This is achieved by enhancing the fidelity of RNA processing, a mechanism that helps cells combat oxidative stress. The study, published in Redox Biology journal, uncovers this novel pathway in gene expression.

In the gene expression process, DNA is transcribed into RNA, which is then translated into proteins responsible for carrying out various cellular functions. Manipulations in these pathways—whether through DNA, RNA, or proteins—can alter gene expression depending on the cellular state. RNA processing, a key pathway controlling gene expression, involves the cleavage of RNA. Interestingly, this cleavage is not always precise, with multiple potential cleavage sites, a phenomenon known as cleavage heterogeneity.
“Controlling oxidative stress is crucial for maintaining cellular health and preventing human diseases. One key way cells regulate oxidative stress is by controlling gene expression through alterations in DNA, RNA, or proteins,” says Dr. Laishram, highlighting the importance of this research in understanding how cells respond to oxidative stress through imprecisions in RNA processing. “This underscores the therapeutic potential of targeting cleavage precision in RNA to mitigate oxidative stress and its associated pathologies.”
Dr. Chandrabhas Narayana, Director of RGCB, described it a significant contribution to understanding how antioxidants influence the pathogenesis and development of diseases.
While previous research had not fully elucidated the mechanism, regulation, or biological implications of cleavage imprecision, this study challenges the common perception that such imprecision is merely error-prone. Dr. Shaji and her team discovered that cleavage imprecision is tightly regulated, playing a critical role in controlling gene expression in response to oxidative stress. Key oxidative stress response genes, such as NQO1, HMOX1, PRDX1, and CAT, show higher heterogeneity compared to genes involved in non-stress responses. Furthermore, the number of cleavage sites on these RNA molecules is reduced, enabling cells to better respond to oxidative stresses.
The RGCB researchers have now shown that this heterogeneity is driven by a fidelity cleavage complex that cleaves RNA at a primary site during oxidative stress. This study marks the first example of the biological significance of cleavage imprecision, which regulates gene expression in the cellular oxidative stress response. The findings offer a novel mechanism of antioxidant response, distinct from other oxidative stress pathways, with far-reaching implications for understanding the pathogenesis of diseases such as cancer, cardiovascular conditions, inflammation, neurodegeneration, aging, and diabetes.
This breakthrough could pave the way for new therapeutic approaches targeting oxidative stress, offering hope for the treatment of a wide range of diseases where antioxidant responses are vital.
Health
PUPS – the AI tool that can predict where exactly proteins are in human cells
Dubbed, the Prediction of Unseen Proteins’ Subcellular Localization (or PUPS), the AI tool can account for the effects of protein mutations and cellular stress—key factors in disease progression.

Researchers from MIT, Harvard University, and the Broad Institute have unveiled a groundbreaking artificial intelligence tool that can accurately predict where proteins are located within any human cell, even if both the protein and cell line have never been studied before. The method – Prediction of Unseen Proteins’ Subcellular Localization (or PUPS) – marks a major advancement in biological research and could significantly streamline disease diagnosis and drug discovery.
Protein localization—the precise location of a protein within a cell—is key to understanding its function. Misplaced proteins are known to contribute to diseases like Alzheimer’s, cystic fibrosis, and cancer. However, identifying protein locations manually is expensive and slow, particularly given the vast number of proteins in a single cell.
The new technique leverages a protein language model and a sophisticated computer vision system. It produces a detailed image that highlights where the protein is likely to be located at the single-cell level, offering far more precise insights than many existing models, which average results across all cells of a given type.
“You could do these protein-localization experiments on a computer without having to touch any lab bench, hopefully saving yourself months of effort. While you would still need to verify the prediction, this technique could act like an initial screening of what to test for experimentally,” said Yitong Tseo, a graduate student in MIT’s Computational and Systems Biology program and co-lead author of the study, in a media statement.
Tseo’s co-lead author, Xinyi Zhang, emphasized the model’s ability to generalize: “Most other methods usually require you to have a stain of the protein first, so you’ve already seen it in your training data. Our approach is unique in that it can generalize across proteins and cell lines at the same time,” she said in a media statement.
PUPS was validated through laboratory experiments and shown to outperform baseline AI methods in predicting protein locations with greater accuracy. The tool is also capable of accounting for the effects of protein mutations and cellular stress—key factors in disease progression.
Published in Nature Methods, the research was led by senior authors Fei Chen of Harvard and the Broad Institute, and Caroline Uhler, the Andrew and Erna Viterbi Professor at MIT. Future goals include enabling PUPS to analyze protein interactions and make predictions in live human tissue rather than cultured cells.
Health
Robot Helps Elderly Sit, Stand, and Stay Safe from Falls
The innovation comes at a time when the United States faces a dramatic demographic shift

As America’s population ages faster than ever before, a team of engineers at MIT is turning to robotics to meet the growing eldercare crisis. Their latest invention, the Elderly Bodily Assistance Robot—or E-BAR—aims to provide critical physical support to seniors navigating life at home, potentially reducing the risk of injury and relieving pressure on a strained care system.
The innovation comes at a time when the United States faces a dramatic demographic shift. The nation’s median age has climbed to 38.9, nearly ten years older than in 1980. By 2050, the number of adults over 65 is projected to surge from 58 million to 82 million. As demand for care rises, the country is simultaneously grappling with shortages in care workers, escalating healthcare costs, and evolving family structures that leave many elderly adults without daily support.
“Eldercare is the next great challenge,” said Roberto Bolli, a graduate student in MIT’s Department of Mechanical Engineering and one of E-BAR’s lead designers, in a media statement. “All the demographic trends point to a shortage of caregivers, a surplus of elderly persons, and a strong desire for elderly persons to age in place.”
E-BAR is designed to address exactly that challenge. The mobile robot acts as a robotic support system, following a user from behind and offering both steadying handlebars and rapid intervention in case of a fall. It can support a person’s full weight and includes side airbags that inflate instantly to catch users if they begin to fall—without requiring them to wear any equipment or harnesses.
“Many older adults underestimate the risk of fall and refuse to use physical aids, which are cumbersome, while others overestimate the risk and may not exercise, leading to declining mobility,” said Harry Asada, the Ford Professor of Engineering at MIT, in a media statement. “Our design concept is to provide older adults having balance impairment with robotic handlebars for stabilizing their body. The handlebars go anywhere and provide support anytime, whenever they need.”
The robot consists of a heavy, 220-pound base equipped with omnidirectional wheels, allowing it to maneuver easily through typical home spaces. From its base, articulated bars extend and adjust to assist users in standing or sitting, and the handlebars provide a natural, unrestrictive grip. In testing, E-BAR successfully helped an older adult complete everyday movements such as bending, reaching, and even stepping over the edge of a bathtub.
“Seeing the technology used in real-life scenarios is really exciting,” said Bolli.
The team’s design, which will be presented later this month at the IEEE Conference on Robotics and Automation (ICRA), aims to eliminate the physical constraints and stigmas often associated with eldercare devices. Their approach prioritizes both independence and safety—key values for aging Americans seeking to remain in their homes longer.
While E-BAR currently operates via remote control, the team plans to add autonomous capabilities and streamline the device’s design for home and facility use. The researchers are also exploring ways to integrate fall-prediction algorithms, developed in a parallel project in Asada’s lab, to adapt robotic responses based on a user’s real-time risk level.
“Eldercare conditions can change every few weeks or months,” Asada noted. “We’d like to provide continuous and seamless support as a person’s disability or mobility changes with age.”
As the nation prepares for the realities of an aging population, MIT’s work offers a glimpse into a future where robotics play a central role in eldercare—enhancing both quality of life and personal dignity for millions of older adults.
Health
Scientist urges need for an Indian-specific blood parameter reference range
In India, standard blood parameter reference ranges aren’t representative of the local population; but based on conclusions derived from population studies in the West.

Prof. Ullas Kolthur-Seetharam, a leading Indian scientist in metabolism and aging, has urged for the re-optimization of standard blood parameter reference ranges to better suit Indian populations, highlighting that current values are based on Western populations and may not account for India-specific factors.
Speaking at the National Technology Day (NTD) 2025 lecture at the Biotechnology Research and Innovation Council-Rajiv Gandhi Centre for Biotechnology (BRIC-R caballoGCB), Kerala, India, Prof. Kolthur-Seetharam emphasized the need for tailored diagnostic benchmarks to improve the accuracy of diagnosing metabolic disorders like diabetes and cardiovascular diseases in India.
“Genetic, dietary, and environmental differences can significantly alter biomarkers,” said Prof. Kolthur-Seetharam, Director of the Centre for DNA Fingerprinting and Diagnostics (BRIC-CDFD), Hyderabad, India. He noted that emerging research reveals how dietary patterns influence health through mitochondrial function and epigenetic regulation, necessitating India-specific reference ranges.
Currently on deputation from the Tata Institute of Fundamental Research (TIFR), Mumbai, Prof. Kolthur-Seetharam has made significant contributions to understanding the interplay of mitochondrial function, epigenetics, and nutrition in shaping health and longevity. He also founded The Advanced Research Unit on Metabolism, Development & Aging (ARUMDA) at TIFR, a pioneering initiative tackling India’s challenges with malnutrition, non-communicable diseases, and aging through interdisciplinary research.
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