James Lawson (Australian doctor)

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Professor

James "Jim" Sutherland Lawson
James Lawson.jpg
James Lawson
Born (1934-05-06) 6 May 1934 (age 89)
Nationality Australian
Education Scotch College, Melbourne
University of Melbourne
Occupation(s)public health doctor and scientist
Known for- research on breast cancer
- originating public health services and prevention programs introduced as a standard part of Australian and international public health services
SpouseMargaret Lawson
Children8 children
Parent(s)Jack and Kitty Lawson
Website www.professor-jameslawson.com

James "Jim" Sutherland Lawson (born 6 May 1934) is an Australian public health doctor and scientist, known for research on breast cancer and for public health services and prevention programs, currently in use in Australian and international public health services.

Contents

Early life

Jim Lawson is the youngest of three children of Jack and Kitty Lawson of Castlemaine, Victoria and the grandson of Harry Lawson, the 27th Premier of Victoria. During the Second World War, Lawson attended the local primary and high school, then he was sent as a boarder to the private Scotch College in Melbourne. Subsequently, he began medical studies at the University of Melbourne, completed with the prize in surgery and a top place as an intern at the Royal Melbourne Hospital. Following his interest in child health, Lawson began training at Melbourne's Royal Children's Hospital.

In 1961, he joined an International Red Cross expedition to the Congo. There he managed together with Gerry Joyce (another Australian surgeon) a District Hospital that had been abandoned by the Belgians following the Congo independence movement and revolution. The context was difficult, as a result of the period of turmoil of those years.

Afterwards, he came back to the children's hospital, where he met (and married nine months later) his future wife, Margaret Ralton.

Papua New Guinea

Soon after their wedding, Lawson and Margaret left for Port Moresby in Papua New Guinea. [1] There he managed the children's ward of the local hospital. Lawson was later awarded a Doctorate in Medicine for his research into the best ways of treating Papuan children suffering from a range of infectious conditions, including pneumonia, diarrhoeal disease and meningitis.

Australian health system management

Lawson and his family returned to Melbourne, following his appointment as Medical Director of the Western General Hospital. He later moved to Hobart, as Director of Tasmanian Hospital and Health Services. During these years, he became involved in activism, writing and publishing reformist books and articles concerning ways of improving the hospital and health system.

In 1974, Lawson was named Director of Health for Northern Sydney. Here he developed a range of innovative services, which were afterwards introduced as a standard part of both Australian and international public health services:

He also introduced a series of public health prevention programs, including

Academia

In 1987 Lawson was recruited by the University of New South Wales and as Head of the School of Public Health, he introduced Master of Public Health programs into the Medical Faculty at this University. During the initial AIDS epidemic of 1983, together with other colleagues, he met and talked to drug users, documenting the sharing of a single intravenous needle as the main factor in the rapid spread of the disease.

Breast and prostate cancer research

In 1998, one of Lawson's post graduate students noted the strikingly lower risk of breast cancer among Asian as compared to Western women and the fact that this risk rose rapidly when Asian women migrated to the West. Lawson initiated further research, the first Australian investigations into viruses as potential causes of human breast cancer. The innovative outcomes of this research are:

This research had shown that human papilloma virus and mouse mammary tumor viruses are present in up to half of all breast cancers in Western women.

Together with his grandmother colleague Wendy Glenn also of the University of New South Wales, Sydney, Australia, he has published evidence that mouse mammary tumour virus and human papilloma virus are highly likely to have causal roles in human breast cancer. Together with Gertrude Buehring of the University of California at Berkeley, Lawson has contributed to research into Bovine leukemia virus which may also have a role in human breast cancer.

Lawson has also worked on the infectious causes of heart attacks. He has published the hypothesis that food and infections combine to initiate atheromatous cardiovascular disease (the origins of heart attacks) in childhood! This is of crucial and ground breaking importance because heart attacks are the biggest killer of all.

Now aged 88, he has a new book to published in late 2022 "Catching Breast Cancer". It will be available on Amazon Kindle.

Books

Lawson has written 9 books, including

YearTitles
1964Paediatric Handbook – The Royal Children's Hospital, Melbourne
1999Breast cancer – can you prevent it
2001Public Health Australia

2022 Catching Breast Cancer to be published by Austin Macauley United Kingdom (available late 2022 Amazon Kindle)

Awards

YearTitles
1961Meritorious Service Award. International Red Cross, Geneva.
1972National Military Service Medal. Anniversary 1951-1972
2002Member of the Order of Australia (AM)

Journal articles

Lawson has written over 200 journal articles

Related Research Articles

<span class="mw-page-title-main">Wart</span> Small, rough growth resembling a cauliflower or a solid blister

Warts are non-cancerous viral growths usually occurring on the hands and feet but can also affect other locations, such as the genitals or face. One or many warts may appear. They are distinguished from cancerous tumors as they are caused by a viral infection, such as a human papillomavirus, rather than a cancerous growth.

<span class="mw-page-title-main">Human papillomavirus infection</span> Human disease

Human papillomavirus infection is caused by a DNA virus from the Papillomaviridae family. Many HPV infections cause no symptoms and 90% resolve spontaneously within two years. In some cases, an HPV infection persists and results in either warts or precancerous lesions. These lesions, depending on the site affected, increase the risk of cancer of the cervix, vulva, vagina, penis, anus, mouth, tonsils, or throat. Nearly all cervical cancer is due to HPV, and two strains – HPV16 and HPV18 – account for 70% of all cases. HPV16 is responsible for almost 90% of HPV-positive oropharyngeal cancers. Between 60% and 90% of the other cancers listed above are also linked to HPV. HPV6 and HPV11 are common causes of genital warts and laryngeal papillomatosis.

<i>Papillomaviridae</i> Family of viruses

Papillomaviridae is a family of non-enveloped DNA viruses whose members are known as papillomaviruses. Several hundred species of papillomaviruses, traditionally referred to as "types", have been identified infecting all carefully inspected mammals, but also other vertebrates such as birds, snakes, turtles and fish. Infection by most papillomavirus types, depending on the type, is either asymptomatic or causes small benign tumors, known as papillomas or warts. Papillomas caused by some types, however, such as human papillomaviruses 16 and 18, carry a risk of becoming cancerous.

Mouse mammary tumor virus (MMTV) is a milk-transmitted retrovirus like the HTL viruses, HI viruses, and BLV. It belongs to the genus Betaretrovirus. MMTV was formerly known as Bittner virus, and previously the "milk factor", referring to the extra-chromosomal vertical transmission of murine breast cancer by adoptive nursing, demonstrated in 1936, by John Joseph Bittner while working at the Jackson Laboratory in Bar Harbor, Maine. Bittner established the theory that a cancerous agent, or "milk factor", could be transmitted by cancerous mothers to young mice from a virus in their mother's milk. The majority of mammary tumors in mice are caused by mouse mammary tumor virus.

<span class="mw-page-title-main">Oncovirus</span> Viruses that can cause cancer

An oncovirus or oncogenic virus is a virus that can cause cancer. This term originated from studies of acutely transforming retroviruses in the 1950–60s, when the term "oncornaviruses" was used to denote their RNA virus origin. With the letters "RNA" removed, it now refers to any virus with a DNA or RNA genome causing cancer and is synonymous with "tumor virus" or "cancer virus". The vast majority of human and animal viruses do not cause cancer, probably because of longstanding co-evolution between the virus and its host. Oncoviruses have been important not only in epidemiology, but also in investigations of cell cycle control mechanisms such as the retinoblastoma protein.

<span class="mw-page-title-main">Papilloma</span> Medical condition

A papilloma is a benign epithelial tumor growing exophytically in nipple-like and often finger-like fronds. In this context, papilla refers to the projection created by the tumor, not a tumor on an already existing papilla.

<span class="mw-page-title-main">Lactiferous duct</span>

Lactiferous ducts are ducts that converge and form a branched system connecting the nipple to the lobules of the mammary gland. When lactogenesis occurs, under the influence of hormones, the milk is moved to the nipple by the action of smooth muscle contractions along the ductal system to the tip of the nipple. They are also referred to as galactophores, galactophorous ducts, mammary ducts, mamillary ducts or milk ducts.

The prolactin receptor (PRLR) is a type I cytokine receptor encoded in humans by the PRLR gene on chromosome 5p13-14. It is the receptor for prolactin (PRL). The PRLR can also bind to and be activated by growth hormone (GH) and human placental lactogen (hPL). The PRLR is expressed in the mammary glands, pituitary gland, and other tissues. It plays an important role in lobuloalveolar development of the mammary glands during pregnancy and in lactation.

Risk factors for breast cancer may be divided into preventable and non-preventable. Their study belongs in the field of epidemiology. Breast cancer, like other forms of cancer, can result from multiple environmental and hereditary risk factors. The term environmental, as used by cancer researchers, means any risk factor that is not genetically inherited.

<span class="mw-page-title-main">Squamous cell papilloma</span> Medical condition

A squamous cell papilloma is a generally benign papilloma that arises from the stratified squamous epithelium of the skin, lip, oral cavity, tongue, pharynx, larynx, esophagus, cervix, vagina or anal canal. Squamous cell papillomas are typically associated with human papillomavirus (HPV) while sometimes the cause is unknown.

<span class="mw-page-title-main">SIM2</span> Protein-coding gene in the species Homo sapiens

Single-minded homolog 2 is a protein that in humans is encoded by the SIM2 gene. It plays a major role in the development of the central nervous system midline as well as the construction of the face and head.

<span class="mw-page-title-main">DKK3</span> Protein-coding gene in the species Homo sapiens

Dickkopf-related protein 3 is a protein in the Dickkopf family that in humans is encoded by the DKK3 gene.

Breast development, also known as mammogenesis, is a complex biological process in primates that takes place throughout a female's life.

<span class="mw-page-title-main">Infectious causes of cancer</span>

Estimates place the worldwide risk of cancers from infectious causes at 16.1%. Viral infections are risk factors for cervical cancer, 80% of liver cancers, and 15–20% of the other cancers. This proportion varies in different regions of the world from a high of 32.7% in Sub-Saharan Africa to 3.3% in Australia and New Zealand.

In molecular biology mir-497 microRNA is a short RNA molecule. MicroRNAs function to regulate the expression levels of other genes by several mechanisms.

Human mammary tumor virus (HMTV) is a B-type retrovirus that is closely related to the mouse mammary tumor virus (MMTV). The existence of this virus was suspected for decades but nucleotide sequences identifying a unique virus in human breast cancer tumors were not confirmed until 2001. Viral particles were isolated several years later. Evidence for a role of HTMV/MMTV in human breast cancer has recently been reviewed.

Breast cancer metastatic mouse models are experimental approaches in which mice are genetically manipulated to develop a mammary tumor leading to distant focal lesions of mammary epithelium created by metastasis. Mammary cancers in mice can be caused by genetic mutations that have been identified in human cancer. This means models can be generated based upon molecular lesions consistent with the human disease.

Janet S Butel is the Chairman and Distinguished Service Professor in the molecular virology and microbiology department at Baylor College of Medicine. Her area of expertise is on polyomavirus pathogenesis of infections and disease. She has more than 120 publications on PubMed. She also has 6 publications in Nature, which is considered one of the most prestigious science journals. She is a member of 9 different organizations and has 13 honors and awards.

mIR489 Non-coding RNA in the species Homo sapiens

MicroRNA 489 is a miRNA that in humans is encoded by the MIR489 gene.

Caroline E. Ford is an Australian scientist at the University of New South Wales and advocate for women in science. Her research aims to understand why gynaecological cancers develop, how they spread and how best to treat them, and she leads the Gynaecological Cancer Research Group at the University of New South Wales, which was established in 2010.

References

  1. Lawson, J.S. (July 2003). "Rethinking McKeown". Am J Public Health. American Journal of Public Health. 93 (7): 1032, author reply 1032–3. doi:10.2105/ajph.93.7.1032. PMC   1447885 . PMID   12835163.
  2. 1 2 Lawson J.S., Leaver, C., Cullen, E.K. (1979). "The Successful Development of Co-ordinated Rehabilitation and Geriatric Services in Northern Sydney". Australian Health Review. 4: 1–10.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. Lawson J.S. (1969). "Management of the Casualty Department. A study at Footscray Hospital". Health Care. 1: 16–18.
  4. Oliver T.I.; Lawson J.S. (1979). "Glass Laceration Injuries and Prevention". Medical Journal of Australia. 1 (5): 190–191. doi:10.5694/j.1326-5377.1979.tb128987.x. PMID   449776. S2CID   22936124.
  5. Oliver T.I.; McFarlane J.P.; Haigh J.C.; Cant G.M.; Bodie A.M.; Lawson J.S. (1981). "Playground Equipment and accidents". Australian Paediatric Journal. 17 (2): 100–103. doi:10.1111/j.1440-1754.1981.tb01914.x. PMID   7305767. S2CID   676961.
  6. Lawson J.S.; Oliver T.I. (1978). "Domestic Swimming Pool Drowning in Children. Positive Results of a Practical Prevention Programme". Australian Paediatric Journal. 14 (4): 275–277. doi:10.1111/j.1440-1754.1978.tb02998.x. PMID   747547. S2CID   12766909.
  7. Rotem T.R.; Lawson J.S.; Wilson S.F.; Engel S.; Rutowski S.B.; Aisbett C.W. (1998). "Severe cervical spinal cord injuries related to rugby union and league football in New South Wales, 1984-1996". The Medical Journal of Australia . 168 (8): 379–381. doi:10.5694/j.1326-5377.1998.tb138989.x. PMID   9594946. S2CID   22747675.
  8. Lawson J.S.; Close G. (1994). "New Public Health' approaches among isolated rural Aboriginal communities in New South Wales". Aboriginal and Torres Strait Islander Information Bulletin. 19: 25–35.
  9. Lawson J.S.; Callaghan A. (1991). "Recreating the village: the successful development of groups as a means of improving social relationships among Australian mothers of new born infants". Australian Journal of Public Health. 15 (1): 64–66. doi:10.1111/j.1753-6405.1991.tb00012.x. PMID   2025679.
  10. Johal H.; Ford C.E.; Glenn W.K.; Heads J.; Lawson J.S.; Rawlinson W.D. (2011). "Mouse mammary tumor like virus (MMTV) sequences in breast milk from healthy lactating women". Breast Cancer Research and Treatment. 129 (1): 149–155. doi:10.1007/s10549-011-1421-6. PMID   21365265. S2CID   24895546.
  11. Heng B.; Glenn W.K.; Lee J.H.K.; Tan X.V.; Lawson J.S.; Whitaker N.J. (2010). "Is HPV-18 present in human breast cancer cell lines?". British Journal of Cancer . 102 (10): 1551–1552. doi:10.1038/sj.bjc.6605672. PMC   2869171 .
  12. Lawson J.S.; Glenn W.K.; Heng B.; Ye Y.; Tran B.; Lutze-Mann L.; Whitaker N.J. (2009). "Koilocytes indicate a role for human papilloma virus in breast cancer". British Journal of Cancer . 101 (8): 1351–1356. doi:10.1038/sj.bjc.6605328. PMC   2768439 . PMID   19773762.
  13. Heng B.; Glenn W.K.; Ye Y.; Tran D.; Delprado W.; Lutze-Mann L.; Whitaker N.J.; Lawson J.S. (2009). "Human papilloma virus is associated with breast cancer". British Journal of Cancer . 101 (8): 1345–1350. doi:10.1038/sj.bjc.6605282. PMC   2737128 . PMID   19724278.
  14. 1 2 Lawson J.S; Heng B. (2010). "Viruses and Breast Cancer". Cancers. 2 (2): 752–772. doi: 10.3390/cancers2020752 . PMC   3835103 . PMID   24281093.
  15. Lawson J.S.; Glenn W.K.; Whitaker N.J. (2008). "Breast cancer, human papilloma virus and sexual activities". British Journal of Cancer . 98 (2): 510–511. doi:10.1038/sj.bjc.6604104. PMC   2361455 .
  16. Lawson J.S.; Heads J.; Glenn W.K.; Whitaker N.J. (2007). "Breastfeeding, breast milk and viruses". BMC Women's Health . 7: 17–20. doi: 10.1186/1472-6874-7-17 . PMC   2148035 . PMID   17919341.
  17. Lawson J.S.; Tran D.D. (2007). "Localised breast cancers may have systemic influences on skin and hair". Journal of Clinical Pathology . 60 (2): 180–184. doi:10.1136/jcp.2006.038158. PMC   1860615 . PMID   16751301.
  18. Lawson J.S.; Tran D.D.; Carpenter E.; Ford C.E.; Rawlinson W.D.; Whitaker N.J.; Delprado W. (2006). "Presence of mouse mammary tumour-like virus gene sequences may be associated with specific human breast cancer morphology". Journal of Clinical Pathology . 59 (12): 1287–1292. doi:10.1136/jcp.2005.035907. PMC   1860546 . PMID   16698952.
  19. Tran D.; Lawson J. (2004). "Rates of estrogen receptor-alpha(ER) expression are no different in low-risk (Vietnam) and high-risk (Australian) breast cancer". Applied Immunohistochemistry & Molecular Morphology. 12 (2): 139–41. doi:10.1097/00129039-200406000-00007. PMID   15354739. S2CID   27316387.