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          <dc:title>Supplementary Figures S1-S6 from Tumor-Secreted ADAMTSL4 Activates Latent TGFβ1 to Drive Cancer Cachexia</dc:title>
          <dc:creator>Juliano Machado (25154222)</dc:creator>
          <dc:creator>Vignesh Karthikaisamy (25154225)</dc:creator>
          <dc:creator>Hermine Mohr (25154228)</dc:creator>
          <dc:creator>Doris Kaltenecker (25154231)</dc:creator>
          <dc:creator>Pia Benedikt (25154234)</dc:creator>
          <dc:creator>Pauline Morigny (25154237)</dc:creator>
          <dc:creator>Amit Mhamane (25154240)</dc:creator>
          <dc:creator>Julia Geppert (25154243)</dc:creator>
          <dc:creator>Amy Rose Fumo (25154246)</dc:creator>
          <dc:creator>Kerstin Haase (14123058)</dc:creator>
          <dc:creator>Estefania Simoes (25154249)</dc:creator>
          <dc:creator>Joanna D.C.C. Lima (18725115)</dc:creator>
          <dc:creator>Anastasia Georgiadi (25154252)</dc:creator>
          <dc:creator>Achim Krüger (25154255)</dc:creator>
          <dc:creator>José Pinhata Otoch (25154258)</dc:creator>
          <dc:creator>Marc E. Martignoni (25154261)</dc:creator>
          <dc:creator>Vickie E. Baracos (25154264)</dc:creator>
          <dc:creator>Mariam Jamal-Hanjani (15386766)</dc:creator>
          <dc:creator>Marilia C.L. Seelaender (25154267)</dc:creator>
          <dc:creator>Olga Prokopchuk (25154270)</dc:creator>
          <dc:creator>Julia Szendrödi (25154273)</dc:creator>
          <dc:creator>Maria Rohm (25154276)</dc:creator>
          <dc:creator>Stephan Herzig (25154279)</dc:creator>
          <dc:creator>Mauricio Berriel Diaz (15037094)</dc:creator>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>Molecular and Cellular Biology</dc:subject>
          <dc:subject>Gastrointestinal Cancers</dc:subject>
          <dc:subject>Colorectal cancer</dc:subject>
          <dc:subject>Lung Cancer</dc:subject>
          <dc:subject>Metabolism</dc:subject>
          <dc:subject>Metabolic pathways</dc:subject>
          <dc:description>&lt;p&gt;Supplementary Fig. S1. ADAMTSL4 is enriched in conditioned media of cachexia-inducing cancer cell lines and is associated with systemic metabolic alterations in patients with cancer. Supplementary Fig. S2. Overexpression of ADAMTSL4 converts non-cachexia-inducing cells into cachexia-inducing cells. Supplementary Fig. S3. Stable knockdown of ADAMTSL4 in cachexia-inducing cells attenuates their muscle-wasting capacity in vitro. Supplementary Fig. S4. Stable knockdown of ADAMTSL4 in cachexia-inducing tumor cells attenuates in vitro and in vivo adipocyte wasting and prolongs cachexia-related survival. Supplementary Fig. S5. ADAMTSL4 targets LAP of latent TGF-β1 complex to promote myotube atrophy via TGF-β latency activation and TGFβR-dependent signaling. Supplementary Fig. S6. ADAMTSL4 induces wasting of murine and human white adipocytes via local activation of TGF-β1–TGFBR1 signaling, without altering circulating TGF-β1 levels.&lt;/p&gt;</dc:description>
          <dc:date>2026-10-01T00:00:00Z</dc:date>
          <dc:type>Text</dc:type>
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          <dc:identifier>10.1158/2159-8290.34040792</dc:identifier>
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          <dc:rights>CC BY</dc:rights>
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