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1 Department of Biotechnology, School of Science, GITAM (Deemed to be University), Visakhapatnam, Andhra Pradesh, 530,045, India; 2 Department of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, IL, 61,801, USA

Correspondence: Sireesha V Garimella; Pankaj Chaturvedi, Email [email protected]; [email protected]

Abstract: Cancer continues to rank among the world’s leading causes of mortality despite advancements in treatment. Cancer stem cells, which can self-renew, are present in low abundance and contribute significantly to tumor recurrence, tumorigenicity, and drug resistance to various therapies. The drug resistance observed in cancer stem cells is attributed to several factors, such as cellular quiescence, dormancy, elevated aldehyde dehydrogenase activity, apoptosis evasion mechanisms, high expression of drug efflux pumps, protective vascular niche, enhanced DNA damage response, scavenging of reactive oxygen species, hypoxic stability, and stemness-related signaling pathways. Multiple studies have shown that mitochondria play a pivotal role in conferring drug resistance to cancer stem cells, through mitochondrial biogenesis, metabolism, and dynamics. A better understanding of how mitochondria contribute to tumorigenesis, heterogeneity, and drug resistance could lead to the development of innovative cancer treatments.

If your mother says she loves you: check it.

A couple weeks ago, I asked Vergecast.

What I was not expecting was for so many people to send me versions of a video that shows a banana getting stitches in a robotic surgery device, with the captions claiming that the surgery is being done remotely over 5G. This video has had an … More.


Meet Dr. Kais Rona, who is as befuddled by the lie appended to his video as anyone else.

The article titled “Evaluation of OVX836: A Promising Universal Influenza Vaccine Candidate” published in The Lancet presents a comprehensive assessment of OVX836, a novel influenza vaccine candidate targeting the nucleoprotein of influenza A virus. Authored by a team of researchers led by IL-R at CEVAC Clinical Unit and Laboratory, the study aims to investigate the safety, immunogenicity, and potential efficacy of OVX836 at different doses, shedding light on its potential as a universal influenza vaccine.

Influenza remains a significant global health concern, with seasonal epidemics and occasional pandemics causing substantial morbidity and mortality. Current influenza vaccines primarily focus on the viral surface protein hemagglutinin, but their efficacy is limited by antigenic variation and the emergence of new strains. Current vaccines are developed for the season based on what strains were prominent in the last season. Additionally, vaccine efficacies can vary from season to season. OVX836 takes a different approach by targeting the highly conserved nucleoprotein, which plays a crucial role in the influenza virus life cycle.

OVX836 elicited a robust immune response, characterized by significant increases in nucleoprotein-specific CD4 and CD8 T-cell responses, as well as the production of anti-nucleoprotein IgG antibodies. The magnitude of these immune responses displayed a dose-dependent relationship, with higher doses of OVX836 leading to stronger immune reactions. Of particular interest was the induction of a CD8 T-cell response, a rare achievement for influenza vaccines and a crucial component of comprehensive immune protection.

“A major highlight of the work is our approach to achieve longevity: using computers to simulate the natural aging system and guide the design and rational engineering of the system to extend lifespan,” Hao told Motherboard. “This is the first time this computationally-guided engineering-based approach has been used in aging research. Our model simulations actually predicted that an oscillator can double the lifespan of the cell, but we were happily surprised that it actually did in experiments.”

The study is part of a growing corpus of mind-boggling research that may ultimately stave off some of the unpleasant byproducts of aging until later in life, while boosting life expectancy in humans overall. Though countless hurdles have to be cleared before these treatments become a reality, Hao thinks his team’s approach could eventually be applied to humans.

“I don’t see why it cannot be applied to more complex organisms,” Hao said. “If it is to be introduced to humans, then it will be a certain form of gene therapy. Of course it is still a long way ahead and the major concerns are on ethics and safety.”

Researchers at the University of Rochester have successfully exported a longevity gene from naked mole rats to mice – a transfer that resulted in both improved health and an extension of the mouse’s lifespan [1].

Longevity. Technology: Naked mole rats, which are known for their long lifespans and exceptional resistance to age-related diseases, have been a focus of longevity research for some time. By introducing a specific gene responsible for improved cellular repair and protection into mice, the Rochester researchers have created promising opportunities to better understand the mechanisms behind aging and potentially increase human lifespan.

“Our study provides a proof of principle that unique longevity mechanisms that evolved in long-lived mammalian species can be exported to improve the lifespans of other mammals,” says Vera Gorbunova, the Doris Johns Cherry Professor of biology and medicine at Rochester [2].

Scientists from the University of Rochester have had the naked mole-rat (Heterocephalus glaber) in their crosshairs for some time, previously identifying how their unique cellular aging mechanisms lay the foundation for their long lifespans – up to 41 years, during which the females also remain fertile – and resistance to age-related diseases.

The modification directly led to the improved overall health of the aging mice and an approximate 4.4% increase in median lifespan.


They weigh about an ounce, spend their lives underground in sub-Saharan Africa and are unlikely to be making the shortlist for any cute animal calendars, but the naked mole-rat continues to show scientists it has incredible age-resistant biology beneath its pale, wrinkly skin.

Building on that knowledge, the researchers genetically modified mice to produce the naked mole-rat version of the hyaluronan synthase 2 gene, which makes a protein that produces high molecular weight hyaluronic acid (HMW-HA). While all mammals have hyaluronan synthase 2, the naked mole-rat’s version is somehow enhanced, driving stronger gene expression.

Inhibiting a protein on the surface of immune cells could offer new strategies for treating severe asthma, Cleveland Clinic researchers found.

Researchers discovered a new way a protein called MCEMP1 contributes to severe inflammation in the airway and lungs. The discovery, published in Nature Communications, provides critical information for developing therapeutic interventions to treat long-term lung conditions, including asthma, on a biological level.

The study was conducted in a lab led by Jae Jung, PhD, chair of the Cancer Biology Department, director of the Infection Biology program, and director of the Sheikha Fatima bint Mubarak Global Center for Pathogen & Human Health Research.