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Tumor-targeting Salmonella typhimurium A1-R overcomes partial carboplatinum-resistance of a cancer of unknown primary (CUP)

  1. Author:
    Miyake, Kentaro
    Kiyuna, Tasuku
    Miyake, Masuyo
    Zhao, Ming
    Wangsiricharoen, Sintawat
    Kawaguchi, Kei
    Zhang, Zhiying
    Higuchi, Takashi
    Razmjooei, Sahar
    Li, Yunfeng
    Nelson, Scott D.
    Russell, Tara
    Singh, Arun
    Murakami, Takashi
    Hiroshima, Yukihiko
    Momiyama, Masashi
    Matsuyama, Ryusei
    Chishima, Takashi
    Singh,Shree Ram
    Chawla, Sant P.
    Eilber, Fritz C.
    Endo, Itaru
    Hoffman, Robert M.
  2. Author Address

    AntiCancer Inc, San Diego, CA 92111 USA.Univ Calif San Diego, Dept Surg, San Diego, CA 92103 USA.Yokohama City Univ, Grad Sch Med, Dept Gastroenterol Surg, Yokohama, Kanagawa, Japan.Univ Calif Los Angeles, Dept Pathol, Los Angeles, CA 90024 USA.Univ Calif Los Angeles, Div Surg Oncol, Los Angeles, CA 90095 USA.Univ Calif Los Angeles, Div Hematol Oncol, Los Angeles, CA USA.NCI, Basic Res Lab, Frederick, MD 21701 USA.Sarcoma Oncol Ctr, 2811 Wilshire Blvd,Suite 414, Santa Monica, CA 90403 USA.
    1. Year: 2018
    2. Date: OCT
    3. Epub Date: 2018 09 14
  1. Journal: TISSUE & CELL
  2. CHURCHILL LIVINGSTONE,
    1. 54
    2. Pages: 144-149
  3. Type of Article: Article
  4. ISSN: 0040-8166
  1. Abstract:

    Cancer of unknown primary (CUP) is metastatic disease without a known primary and therefore very difficult to identify effective therapy. Previously, we demonstrated partial efficacy of Salmonella typhimurium A1-R (S. typhimurium A1-R) alone and carboplatinum alone (CAR) on a CUP patient tumor in the patient-derived xenograft (PDOX) model. The aim of the present study was to investigate the efficacy of S. typhimurium A1-R combined with CAR on the CUP PDOX model. The CUP tumors were implanted orthotopically into the left supraclavicular fossa of nude mice to match the site from which they were resected from the patient. CUP PDOX models were divided randomly into the following 4 groups after the tumor volume reached 100 mm(3): G1: untreated group; G2: CAR (30 mg/kg, i.p., weekly, 2 weeks); G3: S. typhimurium A1-R (5x10(7) CFU/body, i.v., weekly, 2 weeks).; G4: S. typhimurium A1-R combined with CAR (S. typhimurium A1-R; 5x10(7) CFU/body, i.v., weekly, 2 weeks; CAR, 30 mg/kg, i.p., weekly, 2 weeks). Each group comprised 7 mice. All mice were sacrificed on day 15. Tumor volume and body weight were measured twice a week. S. typhimurium A1-R and CAR moderately inhibited tumor growth compared to the untreated group on day 15 (P < 0.001 and P < 0.001, respectively). S. typhimurium A1-R combined with CAR inhibited the tumor growth significantly more compared to S. typhimurium A1-R monotherapy or CAR monotherapy on day 15 (P = 0.004 and P = 0.001, respectively). The present report demonstrates that S. typhimurium A1-R can increase the efficacy of a standard drug used for CUP in a PDOX model.

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External Sources

  1. DOI: 10.1016/j.tice.2018.09.001
  2. PMID: 30309504
  3. WOS: 000446691200019

Library Notes

  1. Fiscal Year: FY2018-2019
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