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Genomic and transcriptomic analyses identify distinctive features of triple-negative inflammatory breast cancer

  • Xiaoping Wang,
  • Li Zhao,
  • Xingzhi Song,
  • Xiaogang Wu,
  • Savitri Krishnamurthy,
  • Takashi Semba,
  • Shan Shao,
  • Mark Knafl,
  • Larry W. Coffer II,
  • Angela Alexander,
  • Anita Vines,
  • Swetha Bopparaju,
  • Wendy A. Woodward,
  • Randy Chu,
  • Jianhua Zhang,
  • Clinton Yam,
  • Lenora W. M. Loo,
  • Azadeh Nasrazadani,
  • Le-Petross Huong,
  • Scott E. Woodman,
  • Andrew Futreal,
  • Ahmed N. Al Rawi,
  • Claudio A. Arrechedera,
  • Kimberly S. Ayers,
  • Claudia Alvarez Bedoya,
  • Elizabeth Burton,
  • Connie A. Chon,
  • Randy Aaron Chu,
  • Shadarra D. Crosby,
  • Jonathan Do,
  • Cibelle Freitas Pinto Lima,
  • Szu-Chin Fu,
  • Andy Futreal,
  • Ana L. Garcia,
  • Celia Garcia-Prieto,
  • Swati Gite,
  • Curtis Gumbs,
  • Kristin J. Hargraves,
  • Meng He,
  • Chacha Horombe,
  • Heladio P. Ibarguen,
  • Stacy Jackson,
  • Jeena Jacob,
  • Mei Jiang,
  • Isha Khanduri,
  • Walter K. Kinyua,
  • Wenhua Lang,
  • Latasha D. Little,
  • Wei Lu,
  • Saradhi Mallampati,
  • Mary Gertrude T. Mendoza,
  • Funda Meric-Bernstam,
  • Mohammad Moustaf Mohammad,
  • Mario Luiz Marques Piubelli,
  • Sabitha Prabhakaran,
  • Kenna R. Shaw,
  • Ping Song,
  • Xiaofei Song,
  • Sandesh Subramanya,
  • Baohua Sun,
  • Shumaila Virani,
  • Wanlin Wang,
  • Ignacio Wistuba,
  • Mingchu Xu,
  • Qingxiu C. Zhang,
  • Shanyu Zhang,
  • Debu Tripathy,
  • Naoto T. Ueno

摘要

Triple-negative inflammatory breast cancer (TN-IBC) is the most aggressive type of breast cancer, yet its defining genomic, molecular, and immunological features remain largely unknown. In this study, we performed the largest and most comprehensive genomic and transcriptomic analyses of prospectively collected TN-IBC patient samples from a phase II clinical trial (ClinicalTrials.gov, NCT02876107, registered on August 22, 2016) and compared them to similarly analyzed stage III TN-non-IBC patient samples (ClinicalTrials.gov, NCT02276443, registered on October 21, 2014). We found that TN-IBC tumors have distinctive genomic, molecular, and immunological characteristics, including a lower tumor mutation load than TN-non-IBC, and an association of immunosuppressive tumor-infiltrating immune components with an unfavorable response to neoadjuvant chemotherapy. To our knowledge, this is the only study in which TN-IBC and TN-non-IBC samples were collected prospectively. Our analysis improves the understanding of the molecular landscape of the most aggressive subtype of breast cancer. Further studies are needed to discover novel prognostic biomarkers and druggable targets for TN-IBC.