The microtubule targeting agent ST-401 triggers cell death in interphase and prevents the formation of polyploid giant cancer cells

• Published in: Journal of translational medicine 2024-05, Vol.22 (1), p.441-441, Article 441
• Main Authors: Vicente, Juan Jesus, Khan, Kainat, Tillinghast, Grant, McFaline-Figueroa, José L, Sancak, Yasemin, Stella, Nephi
• Format: Article
• Language: English
• Subjects: Analysis; Apoptosis; Biochemistry; Cancer; Cancer cells; Cell death; Cell Death - drug effects; Cell Line, Tumor; Energy Metabolism - drug effects; Gene Expression Regulation, Neoplastic - drug effects; Giant Cells - drug effects; Giant Cells - metabolism; Giant Cells - pathology; Glioblastoma - drug therapy; Glioblastoma - genetics; Glioblastoma - metabolism; Glioblastoma - pathology; Health aspects; Homeopathy; Humans; Interphase - drug effects; Materia medica and therapeutics; Microtubules; Microtubules - drug effects; Microtubules - metabolism; Mitochondria - drug effects; Mitochondria - metabolism; Mitochondrial Dynamics - drug effects; Neoplasms - drug therapy; Neoplasms - genetics; Neoplasms - metabolism; Neoplasms - pathology; Physiological aspects; Polyploidy; Prevention; RNA; RNA sequencing; Therapeutics; Vincristine
• ISSN: 1479-5876; 1479-5876
• DOI: 10.1186/s12967-024-05234-3

Microtubule targeting agents (MTAs) are commonly prescribed to treat cancers and predominantly kill cancer cells in mitosis. Significantly, some MTA-treated cancer cells escape death in mitosis, exit mitosis and become malignant polyploid giant cancer cells (PGCC). Considering the low number of cancer cells undergoing mitosis in tumor tissues, killing them in interphase may represent a favored antitumor approach. We discovered that ST-401, a mild inhibitor of microtubule (MT) assembly, preferentially kills cancer cells in interphase as opposed to mitosis, a cell death mechanism that avoids the development of PGCC. Single cell RNA sequencing identified mRNA transcripts regulated by ST-401, including mRNAs involved in ribosome and mitochondrial functions. Accordingly, ST-401 induces a transient integrated stress response, reduces energy metabolism, and promotes mitochondria fission. This cell response may underly death in interphase and avoid the development of PGCC. Considering that ST-401 is a brain-penetrant MTA, we validated these results in glioblastoma cell lines and found that ST-401 also reduces energy metabolism and promotes mitochondria fission in GBM sensitive lines. Thus, brain-penetrant mild inhibitors of MT assembly, such as ST-401, that induce death in interphase through a previously unanticipated antitumor mechanism represent a potentially transformative new class of therapeutics for the treatment of GBM.