What does this research mean for the field?

Aging protects against brain metastasis in lung cancer by activating MT1G/NF-κB signaling in brain astrocytes, which increases SPARC secretion and inhibits tumor-promoting ITGB1 signaling. Novelty: ClaimNovelty.NOVEL_FINDING. Consensus alignment: ConsensusAlignment.NEUTRAL.

What question did this study set out to answer?

This research aims to explore the relationship between aging and the incidence of brain metastasis in lung cancer patients.

April 5, 2026

Abstract 2079: Aging attenuates brain metastasis in lung cancer through the MT1G/NF-κB/SPARC signaling.

Key Points

This research aims to explore the relationship between aging and the incidence of brain metastasis in lung cancer patients.
Analyzed brain metastasis cases in lung cancer patients using the SEER cancer registry.
Investigated molecular mechanisms involving MT1G/NFκB signaling and SPARC secretion in astrocytes.
Examined therapeutic effects of ITGB1 targeting using liposome-encapsulated SPARC peptide.
Found a significantly lower incidence of brain metastasis in older lung cancer patients compared to younger patients.
Identified activation of MT1G/NFκB signaling in reactive astrocytes as a protective mechanism.
Demonstrated that targeting ITGB1 with SPARC peptides effectively suppresses tumor growth and metastasis.

Abstract

Abstract Aging is a major risk factor for cancer, with incidence and mortality increasing significantly with age across most cancer types. With the global population aged over 60 projected to rise from 12-22 percent by 2050, understanding the relationship between aging and cancer is critically important. Aging and cancer share several hallmarks—including cumulative genetic damage, immune senescence, altered nutrient sensing, and chronic low-grade inflammation. This overlap implies that age-related biological changes may not only correlate with increased cancer incidence but also influence tumor progression and metastasis. Despite this preconceived notion, population-based epidemiological studies have revealed an inverse association between aging and brain metastasis incidence in lung cancer, with unclear molecular mechanism(s). Here, we show a significantly lower incidence of brain metastasis in aged lung cancer patients compared to younger patients or those with brain metastasis from other cancers, based on analysis of the SEER population-based cancer registry. Mechanistically, aging activates MT1G/NFκB signaling in reactive astrocytes within the brain, leading to increased secretion of SPARC from A1 type reactive astrocytes, which suppresses tumor growth by inhibiting ITGB1 signaling in tumor cells, thereby limiting brain colonization. Notably, therapeutic targeting of ITGB1 using liposome-encapsulated SPARC peptide effectively suppresses brain tumor growth and metastasis, supporting its tumor-suppressive role. These findings uncover an age-associated protective mechanism and provide a compelling rationale for developing targeted therapies to prevent or treat brain metastasis in younger lung cancer patients. Citation Format: Abhishek Tyagi, Shih-Ying Wu, Jee Won Kim, Kerui Wu, Ravindra Deshpande, Kounosuke Watabe. Aging attenuates brain metastasis in lung cancer through the MT1G/NF-κB/SPARC signaling abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2079.

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