Cancer Heterogeneity and Plasticity ISSN 2818-7792

Special Issue

Targeting the Heterogeneous and Plastic Tumor Ecosystem in Prostate Cancer—A Special Issue Dedicated to Dr. Leland W. Chung

Manuscript Submission Deadline: December 30, 2026 Submit Now

Guest Editors
  • Dean G. Tang
    Dean G. Tang

    Distinguished Professor and Chair, Department of Pharmacology & Therapeutics, Roswell Park Comprehensive Cancer Center (RPCCC), USA

    Research Interests: Cancer cell heterogeneity and plasticity; cancer stem cells; prostate cancer; non-coding RNAs and epigenetic regulation of cell state

    E-Mail | Website
  • James L. Mohler
    James L. Mohler

    Professor, Department of Urology, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA

    E-Mail | Website
  • Jer-Tsong Hsieh
    Jer-Tsong Hsieh

    Professor, Department of Urology, UT Southwestern Medical Center, Dallas, TX 75390, USA

    E-Mail | Website
Introduction
Human cancers represent a live ecosystem. Both primary tumors and disseminated diseases are comprised of malignant and benign cells in the tumor microenvironment or TME. Cancer cells, non-cancer cells, and non-cellular components (e.g., extracellular matrix or ECM, ECM rigidity or stiffness, interstitial fluid volume and pressure, inflammatory cytokines, oxygen tension, and nutrient availability) in the TME constantly interact to drive tumor evolution and progression. Both the cancer parenchyma and TME should be targeted holistically to achieve enduring therapeutic efficacy and hence long-lasting clinical benefits.
The concept that non-malignant cells and the environment (e.g., chronic inflammation) surrounding the tumor parenchyma may play a role in aiding tumor development and cancer progression was proposed by the pathologist Rudolf Virchow in the 1860s. However, it is the pioneering work from scientists including Dr. Leland W.K. Chung to experimentally demonstrate the essential and causal functions of stromal cells and stromal components in facilitating tumor growth and cancer metastasis. Dr. Chung, a scientific giant working primarily on prostate cancer, was among the first to evince the importance of tumor stroma in driving prostate cancer progression and bone metastasis. Please visit https://ascopost.com/issues/august-25-2021/leland-chung-dies-at-80/ and https://urologichistory.museum/the-scope-of-urology-newsletter/issue-6-summer-2021/leland-w.-chung-phd-(1940-2021) for an appreciation of Dr. Chung’s scientific legacy.
Prostate cancer is a disease of aging; the incidence increases dramatically in men over 50-55 years old and prostate cancer is the most common non-cutaneous cancer in men in the U.S and most other developed countries. Currently, the mortality rate of prostate cancer is second to that of lung cancer. Most of the cancer-related deaths are caused by metastatic disease. One of the most exciting developments in modern medicine has been the step-by-step re-construction of the disease in combination with molecular analysis of genetics, cell biology, and animal models. Dr. Chung is recognized as an early pioneer in establishing the importance of stromal-epithelial interactions by unveiling the key role of androgen receptor in the stroma in driving prostate gland development. His later work in prostate cancer advanced the concept of a “vicious cycle” between prostate cancer and its microenvironment; he demonstrated the critical role of TME in driving progression to androgen independency and metastasis to bone. As an example, the C4-2/C-42B model, developed by Dr. Chung, is among the most widely used in the field for modeling castration resistance in the context of clonal selection and understanding therapy-driven cellular plasticity. As another example, the metastatic prostate cancer patient-derived ARCaP cell model, developed by Dr. Chung, represents the full spectrum of cancer cell heterogeneity and was used demonstrate the functional roles of epithelial-mesenchymal transition and androgen receptor reprogramming to promote prostate cancer progression.
Dr. Chung used many of the unique models developed in his lab, to advocate for the novel concept of “osteomimicry”, which is now recognized as the manifestation of lineage-plastic properties of carcinoma cells that migrate to, and proliferate in, the skeleton. In addition, Dr. Chung’s group demonstrated critical roles for a variety of extracellular matrix, cytokine, and signaling factors to orchestrate tumor growth and metastasis. For example, they reported a new model of “cancer tropism” involv¬ing the bone cytokine RANK-L, which is capable of driving indolent prostate cancer cells to the bone and prostate cancer cells expressing RANK-L can act as powerful metastasis-initiating cells, which then attract low-metastatic cells to the bone metastatic sites.
In brief summary, Dr. Chung has made major scientific discoveries in understanding prostate cancer biology and demonstrating the indispensable roles of heterotypic cancer cell-stromal interactions in driving bone metastasis and for developing new imaging technologies for cancer diagnosis and new gene therapies to kill metastatic prostate cancer cells.
We dedicate this Special Issue of CHP to recognize Dr. Chung’s scientific achievement and celebrate his legacy.
Manuscript Submission Information

Submitted manuscripts should not have been published previously, nor been under consideration for publication elsewhere (except conference proceedings). All manuscripts will be thoroughly refereed through a single-blinded peer-review process. A guide for manuscript submission is available at Submission Instructions.

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