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From Melanocytes to Melanoma: The Progression to Malignancy
 
 
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From Melanocytes to Melanoma: The Progression to Malignancy [Hardcover]

Vincent J. Hearing (Editor), Stanley P. L. Leong (Editor)
5.0 out of 5 stars  See all reviews (1 customer review)

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Book Description

1588294595 978-1588294593 December 15, 2005 1
Leading researchers and clinicians join forces to explain how malignant melanoma develops from its benign precursor cell type. The authors focus on the molecular mechanisms involved in melanogenesis, in the malignant transformation of melanocytes, and in the further progression of primary melanomas into invasive and metastatic melanomas. They also review recent advances in our understanding of the basic biology of melanocytes and the development, migration, and differentiation of melanoblasts into melanocytes. The book provides an up-to-date understanding of the progressive mechanisms of oncological development in malignant melanoma, a likely model of malignant progress for other types of cancer, and the ongoing development of novel therapeutics.

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Editorial Reviews

Review

From the reviews:

"...this compendium of current thinking is recommended reading for anyone with an interest in pigmentation and cancer and a valuable resource for any library." -Melanoma Research

"This book, the first of its kind on melanoma, details the current state of our knowledge … . should be viewed as an important resource for understanding the broad field of melanocyte and melanoma biology. Newcomers to the field … will find this book extremely useful. … This book captures the tremendous progress made in the field … . It is a valuable resource for biologists and basic scientists … as well as for pathologists; dermatologists, surgeons, and medical oncologists … ." (Lynn M. Schuchter, The New England Journal of Medicine, March, 2007)

"...captures the tremendous progress made in the field...will help to propel the field to new successes...a valuable resource for biologists and basic scientists interested in the biology of pigment cells as well as for pathologists, dermatologists, surgeons, and medical oncologists interested in the diagnosis and treatment of melanoma." -New England Journal of Medicine

"The editors have compiled a highly prestigious group of authors, who are leaders in the field of melanocyte and melanoma research, to present a very comprehensive exposition of the current knowledge of melanocyte biology and melanoma. … As a clinical researcher, I found … it fascinating, yielding a tremendous appreciation for the meticulous and extensive work that has been done to date, some of which has and more of which will very likely provide leads to clinical interventions." (Janice P. Dutcher, Medical Oncology, Vol. 23 (3), 2006)

"An extremely detailed book on each of the various pathways, growth factors, and oncogenes affecting the melanocyte. This is a comprehensive review and … physicians such as dermatologists, pathologists, and oncologists will find it helpful. It is very thorough in its presentation of cellular events … . This book will serve primarily as a reference for basic scientists and biologists. Physician scientists will also use the book. Clinicians may find the book highly detailed, with more information then they require." (Mary C. Martini, Doody’s Review Service, July, 2006)

From the Back Cover

Melanoma offers an excellent model for cancer biology and an opportunity to understand the progression of a normal skin cell-the melanocyte-to malignancy. In From Melanocytes to Melanoma: The Progression to Malignancy, leading researchers and clinicians join forces to explain how skin cancer develops from its benign precursor cell type. The authors focus on the molecular mechanisms involved in melanogenesis, the malignant transformation of melanocytes, and the further progression of primary melanomas into invasive and metastatic melanomas. They also review recent advances in our understanding of the basic biology of melanocytes and the development, migration, and differentiation of melanoblasts into melanocytes. The text is augmented by four color plates.
Comprehensive and illuminating, From Melanocytes to Melanoma: The Progression to Malignancy, provides pathologists, dermatologists, surgeons, and medical oncologists with an up-to-date understanding of the progressive mechanisms of oncological development in malignant melanoma, a likely model of malignant progress for other types of cancer, and the ongoing development of novel therapeutics.

Product Details

  • Hardcover: 696 pages
  • Publisher: Humana Press; 1 edition (December 15, 2005)
  • Language: English
  • ISBN-10: 1588294595
  • ISBN-13: 978-1588294593
  • Product Dimensions: 10.2 x 7.2 x 1.6 inches
  • Shipping Weight: 4.1 pounds (View shipping rates and policies)
  • Average Customer Review: 5.0 out of 5 stars  See all reviews (1 customer review)
  • Amazon Best Sellers Rank: #1,510,249 in Books (See Top 100 in Books)

 

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5.0 out of 5 stars A Great Overview of Melanoma and Its Pathways, July 22, 2011
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This review is from: From Melanocytes to Melanoma: The Progression to Malignancy (Hardcover)
Hearing and Leong have prepared an excellent review of the state of the art in the underlying genetic mechanisms involved in melanoma. The book is a lengthy but highly readable collection of chapters prepared by major contributors to the field.

The Editors state that the text is divided into three sections:

Part I: Development of melanocytes
Part II: Melanocyte Transformation to Melanoma
Part III: Primary Invasive Melanoma to Metastasis

Thus the authors try to follow the steps from development, transition and metastasis. In so doing the focus is on pathways, transcription factors, and the genetic errors which cause failure in normal homeostatic management of the melanocyte.

The strength of the text is its breath of authors and their insight. That also is its weakness since there is considerable overlap and some discussions are often just a bit too brief.

In Part I there is an excellent set of presentations on the development and life cycle of the melanocyte. As with the entire work there is primary focus on the cell and its internal pathways.

For example Chapter 3 is an excellent discussion of MITF, the signalling that facilitates it via '-catenin, and its impact on melanocyte lineage. This provides an introduction of the LEF/TCF transcription factors which will play a role again and again.

In Part II there are extensive chapters on the progression from melanocyte to melanoma. Chapter 7 is an excellent review of the signalling changes in melanoma.

Wnt5a is discussed at length in Chapter 7 and also there is an introduction to BRAF as well. Most of the key pathways and their constituents are discussed, and this adds to what has previously been introduced. The graphics are quite useful and the result provides the reader with a focus on the specifics of melanoma. To those familiar with these pathways from other cancers then there is a considerable amount of overlap, especially on seeing PTEN as a common factor.

Chapter 9 is a critical chapter for the understanding of melanoma. The E-cadherins are the proteins which bind the melanocytes to the keratinocytes in the basal layer. This chapter discusses what happens as they lose their ability and are replaced by N-cadherins. The melanocyte no longer adheres to where it is supposed to and starts wandering. That is one of the characteristics of a malignancy common to all cancers. It is especially well described in this Chapter.

Chapter 11 describes the initiation of melanoma as a process. On p 189 there is the common Vogelstein stepped process gong from a benign melanocyte thru dysplasia and on to SSM and Vertical phase and metastasis. The author clearly states that the steps may not occur sequentially. Thus the normal thought of E-cadherin loss being a final step may actually be a step occurring in say a melanoma in situ, although that is still speculative. The questions left unanswered are still what specific changes caused what mutations where and what is the common sequence.

Part III looks at the issue of metastasis with emphasis on pathway elements. This is an extensive discussion of where the literature was at when published but does not reflect the progress made with BRAF and its management, limited as it may still be.

Chapter 31 raises a key issue worthy of further discussion. Namely, the classic way a patient approaches this process is first a visit to a general practice or family physician, then a referral to a dermatologist who removes the suspected lesion, which is sent hopefully to a dermatopathologist who treats and processes the lesion. If positive for melanoma then after a few more meetings the patient may be referred to a melanoma specialist. By then the ability to determine many of the genetic markers useful for determining the prognosis have been lost. The authors make several clear points on this issue which may become a more significant factor in treatment as we go forward.

Some topics worth discussing but not included in my opinion are:

Stem Cell Issues: What of the stem cell theory and how does it apply to melanoma. There is some discussion on stem cells and growth factors but the broader issue of there being a stem cell is not covered.

Dynamics of Pathways: How do these pathways change in time. This is the dynamics of pathways. There is a reference to the use of differential equations to understanding them but it would have been useful to have included some specific discussions in a separate chapter.

Dynamics of Mutations and Cell Alterations: What happens when, namely there should be a discussion of the steps leading to specific changes leading to the pathway changes and then to a malignancy.

Methylation, microRNAs and other Epigenetic Factors in Changing Expressions: There is some discussion on methylation but none that I could see on microRNAs or other epigenetic factors. There is a considerable body of knowledge developing and its inclusion would have been useful

SNPs and Their usefulness in Identifying Malignancy:

Specific Approaches to Treatment; Immunological and Pathway Targeting: This is the best place to have introduced the BRAF treatment. Also there has been decades of work on the immunological side and it is covered somewhat.

Some of the minor apparent weaknesses of the book are:

Multiple Authors with Multiple Repeats: This is a good and bad issue. The book is a collection of writings by multiple specialists and each is superbly done.

Dated: Like any work in this field it gets aged quickly. For example all of the recent work on BRAF and its treatment postdates the work although it is clearly anticipated.

Detail: Since each author somewhat repeats and begins again, there could have been more depth in each chapter if there had been tighter coordination. This is a nit but it is the constant challenge of a collaborative work. Notwithstanding this really is a desire to have it expand.

Overall this is a superb contribution and an essential work to be on the desk of anyone examining pathways and cancer.
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Inside This Book (learn more)
First Sentence:
The neural crest cells initially form as the neural tube is closing: at 8 d of gestation in mice and at 22 d in humans. Read the first page
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Biol Chem, Invest Dermatol, Pigment Cell Res, Melanoma Res, Nat Genet, Genes Dev, Mol Cell Biol, Proc Natl Acad Sci, Clin Oncol, Hum Genet, Hum Mol Genet, Dev Biol, Proc Nall Acad Sci, Humana Press Inc, New York, Proc Nail Acad Sci, Arch Dermatol, Natl Cancer Inst, Nucleic Acids Res, Cell Sci, Med Genet, Ann Surg, Hum Pathol, Biochem Biophys Res Commun, Cutan Pathol
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